N. Nevin

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Cytogenetic analysis on children born of parents treated with immunosuppressive drugs.

M. Mcgeown, N. Nevin, 1978, Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association.

Potato avoidance during pregnancy in women with a previous infant with either anencephaly and/or spina bifida.

N. Nevin, J. Merrett, 1975, British journal of preventive & social medicine.

Comparison of central nervous system malformations in spontaneous absortions in Northern Ireland and south-east England.

N. Nevin, J. Merrett, J. MacHenry, 1979, British medical journal.

Apparent prevention of neural tube defects by periconceptional vitamin supplementation.

A. Read, M. Seller, R. Harris, 1981, Archives of disease in childhood.

Factors associated with anencephalus and spina bifida in Belfast.

J. Elwood, N. Nevin, 1973, British journal of preventive & social medicine.

APO E Genotype and Familial Hypercholesterolaemia

I. Young, C. Graham, E. Duly, 1997, Annals of clinical biochemistry.

A novel single base deletion in the LDLR gene (211delG): Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes.

I. Young, C. Graham, D. Nicholls, 1996, Atherosclerosis.

Galton's ‘Law of Ancestral Heredity’: Its Influence on the Early Development of Human Genetics

P. Froggatt, N. Nevin, 1971, History of science; an annual review of literature, research and teaching.

A Molecular Variant of Angiotensinogen Is Associated With Diabetic Nephropathy in IDDM

A. Maxwell, A. Hughes, N. Nevin, 1996, Diabetes.

Genetic study of congenital heart defects in Northern Ireland (1974-1978).

N. Nevin, J. Nelson, E. J. Hanna, 1994, Journal of medical genetics.

Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysis.

A. Green, T. Sepp, J. Yates, 1997, Human molecular genetics.

Non‐phenylketonuria hyperphenylalaninaemia in Northern Ireland: Frequent mutation allows screening and early diagnosis

C. Graham, J. Zschocke, N. Nevin, 1994, Human mutation.

Characterization of human skin fibroblast extracellular proteins by two‐dimensional polyacrylamide gel electrophoresis

C. Graham, A. Hughes, N. Nevin, 1988, Electrophoresis.

Diagnostic and genetical aspects of tuberous sclerosis.

N. Nevin, W. Pearce, 1968, Journal of medical genetics.

ACE gene typing

A. Maxwell, N. Nevin, D. Fogarty, 1994, The Lancet.

Prenatal diagnosis of the Meckel syndrome

N. Nevin, W. Thompson, G. Davison, 1979, Clinical genetics.

Ullrich-Turner syndrome: seven pregnancies in an apparent 45,X woman.

M. Armstrong, A. Magee, N. Nevin, 1998, American journal of medical genetics.

Northern Ireland

N. Nevin, W. Johnston, P. Morrison, 2020, Adoption & Fostering.

DNA storage and duplicate sampling: lessons learnt from testing for Huntington's disease.

C. Graham, P. Morrison, N. Nevin, 1993, Journal of medical genetics.

Relation of alpha-1-antitrypsin phenotype to the performance of pulmonary function tests and to the prevalence of respiratory illness in a working population.

N. Nevin, J. Merrett, W. Johnston, 1976, Thorax.

phenotype to theperformance ofpulmonary function tests andtotheprevalence ofrespiratory illness ina working population

N. Nevin, J. Merrett, W. Johnston, 1976 .

Guidelines for Follow-Up of Women at High Risk for Inherited Breast Cancer: Consensus Statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

J. Chang-Claude, K. Heimdal, P. Møller, 2002, Disease markers.

Hyperlipidaemic xanthomatosis. I. Increased risk of death from ischaemic heart disease in first degree relatives of 53 patients with essential hyperlipidaemia and xanthomatosis.

N. Nevin, J. Slack, 1968, Journal of medical genetics.

Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland.

C. Graham, P. Morrison, N. Nevin, 1993, Journal of medical genetics.

Significant linkage disequilibrium between the Huntington ' s disease locus and markers at loci D 4 S 1 O , D 4 S 95 , and D 4 S 111 in Northern Ireland

C. Graham, P. Morrison, N. Nevin, 2022 .

Hyperlipidaemic xanthomatosis. II. Mode of inheritance in 55 families with essential hyperlipidaemia and xanthomatosis.

N. Nevin, J. Slack, 1968, Journal of medical genetics.

Prevalence and survival of patients with cystic fibrosis in Northern Ireland, 1961-1971.

N. Nevin, A. Redmond, G. B. Nevin, 1983, The Ulster medical journal.

Idiopathic intestinal pseudo‐obstruction: A familial visceral neuropathy

N. Nevin, H. Bharucha, G. Odling‐Smee, 1980, Clinical genetics.

Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approach.

C. Graham, J. Zschocke, N. Nevin, 1995, American journal of human genetics.

Prevention and avoidance of congenital malformations.

N. Nevin, 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Aglossia-adactylia syndrome.

N. Nevin, D. Burrows, G. Allen, 1970, Oral surgery, oral medicine, and oral pathology.

Aglossia-adactylia syndrome.

N. Nevin, D. Burrows, G. Allen, 1975, Journal of medical genetics.

Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland.

J. Uitto, K. Mckenna, C. Munro, 1998, The Journal of investigative dermatology.

Alpha1 antitrypsin phenotypes in Northern Ireland

N. Nevin, G. Blundell, A. Frazer, 1975, Annals of human genetics.

Royal academy of medicine in Ireland section of dermatology

B. Bresnihan, W. Irwin, D. Veale, 1992 .

Identification of a frameshift mutation (557 del T) in exon 4 of the CFTR gene.

C. Graham, N. Nevin, A. Hill, 1992, Genomics.

Duchenne muscular dystrophy in a female with a translocation involving Xp21.

N. Nevin, A. Hughes, J. Lim, 1986, Journal of medical genetics.

Case Duchenne muscular dystrophy in a female with a translocation involving Xp2l

N. Nevin, A. Hughes, M. CALWELLt, 2022 .

T-cell receptor alpha, beta, gamma, and delta chain gene microsatellites show no association with multiple sclerosis

C. Graham, S. Mcmillan, S. Hawkins, 1996, Neurology.

Familial expansile osteolysis. A new dysplasia.

J. Kanis, R. Mollan, J. Sloan, 1988, The Journal of bone and joint surgery. British volume.

The Epidemiology of Myotonic Dystrophy in Northern Ireland

A. Magee, N. Nevin, 2000, Public Health Genomics.

THE IMPACT OF LIFELONG CARING IN IRELAND

P. W. Johnston, M. I. Halliday, D. Mccluskey, 2008 .

Gene therapy advisory committee: long-term monitoring of patients participating in gene therapy: Health Departments of the United Kingdom.

N. Nevin, J. Spink, Norman C Nevin, 2000, Human gene therapy.

Three novel mutations in the EGF precursor homology domain of the low‐density lipoprotein receptor gene in Northern Irish patients with familial hypercholesterolemia

I. Young, C. Graham, D. Nicholls, 1995, Human mutation.

Royal academy of medicine in ireland section of dermatology

R. O'Moore, E. Healy, G. Murphy, 1993 .

A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-Meara.

K. Mckenna, A. Irvine, A. Hughes, 1997, The Journal of investigative dermatology.

The STR system in the human phenylalanine hydroxylase gene: true fragment length obtained with fluorescent labelled PCR primers

C. Graham, J. Zschocke, N. Nevin, 1994, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities.

S. Dhanjal, A. Szczepura, M. Hultén, 2003, Health technology assessment.

Myelocele and alpha-fetoprotein in amniotic fluid.

N. Nevin, W. Thompson, S. Nesbitt, 1973, Lancet.

Report of the third international workshop on human chromosome 18 mapping 1995 Prepared by J . Overhauser , 1

K. Kidd, T. Marr, D. Meyers, 2018 .

Lack of association between myelin basic protein gene microsatellite and multiple sclerosis

C. Graham, S. Hawkins, N. Nevin, 1993, The Lancet.

Congenital anomalies in twins in Northern Ireland. III: Anomalies of the cardiovascular system, 1974-1978.

N. Nevin, J. Little, 1989, Acta geneticae medicae et gemellologiae.

Linkage Diseq uiiibrium Between the CA M icrosatellite

N. Nevin, A. Hughes, K. Larkin, 1994 .

Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis.

W. Reardon, R. Winter, S. Malcolm, 1997, Journal of medical genetics.

Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia.

N. Nevin, H. Mulholland, P. S. Thomas, 1996, American journal of medical genetics.

Three Cases of Intravascular Thrombosis Occurring in Patients Receiving Oral Contraceptives

P. Elmes, N. Nevin, J. Weaver, 1965, British medical journal.

Hereditary breast cancer in Northern Ireland.

N. Nevin, R. Spence, S. Russell, 1996, The Ulster medical journal.

Association between holoprosencephaly and exposure to topical retinoids: results of the EUROCAT Survey.

E. Calzolari, P. De Wals, M. Cornel, 1991, Paediatric and perinatal epidemiology.

Exponential increase in the Huntington disease gene in a three-generation family

J. McMenamin, P. Morrison, N. Nevin, 1999 .

Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).

P. Morrison, N. Nevin, 1996, Journal of medical genetics.

Phenylketonuria and the peoples of Northern Ireland

J. Mallory, J. Zschocke, H. Eiken, 1997, Human Genetics.

Antenatal detection of grossly distended bladder owing to absence of the urethra in a fetus with trisomy 18.

N. Nevin, J. Nevin, M. Gray, 1983, Journal of medical genetics.

Recurrent neural tube defects, risk factors and vitamins.

A. Read, M. Seller, R. Harris, 1986, Archives of disease in childhood.

ATYPICAL ERYTHROKERATODERMA WITH DEAFNESS, PHYSICAL RETARDATION AND PERIPHERAL NEUROPATHY

I. Allen, P. Froggatt, N. Nevin, 1972, The British journal of dermatology.

Cardiovascular abnormalities in the oculo-auriculo-vertebral spectrum (Goldenhar syndrome).

B. Craig, P. Morrison, N. Nevin, 1992, American journal of medical genetics.

Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome.

N. Nevin, P. S. Thomas, J. Hutchinson, 1986, American journal of medical genetics.

Genetics in reproduction

N. Nevin, N. O’Hanrahan, 1984 .

Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation).

M. Petzl-Erler, D. Housman, R. Maas, 1994, Genomics.

Syndrome of partial aniridia, cerebellar ataxia, and mental retardation--Gillespie syndrome.

N. Nevin, J. Lim, 1990, American journal of medical genetics.

The 'law of ancestral heredity' and the Mendelian-ancestrian controversy in England, 1889-1906.

P. Froggatt, N. Nevin, 1971, Journal of medical genetics.

Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.

D. Eedy, N. Nevin, P. S. Thomas, 1995, Journal of medical genetics.

Melorheostosis in a family with autosomal dominant osteopoikilosis.

N. Nevin, G. Cowie, P. S. Thomas, 1999, American journal of medical genetics.

Is antenatal selection for spina bifida possible?

N. Nevin, L. Boydell, 1990, BMJ.

Cytogenetic investigations in a family with ataxia telangiectasia

M. Humphreys, N. Nevin, M. Wooldridge, 1989, Human Genetics.

Quantitative nitroblue tetrazolium test in mongolism.

J. B. Bridges, N. Nevin, N. Johnston, 1975, Irish journal of medical science.

Raised alpha-fetoprotein levels in amniotic fluid and maternal serum associated with distension of the fetal bladder caused by absence of urethra.

N. Nevin, F. McKeown, A. Ritchie, 1978, Journal of medical genetics.

Transplacental early amniocentesis and pregnancy outcome

N. Nevin, S. Tharmaratnam, J. Dornan, 1998, British journal of obstetrics and gynaecology.

RAISED ALPHA‐FETOPROTEIN LEVELS IN AMNIOTIC FLUID AND MATERNAL SERUM IN A TRIPLET PREGNANCY IN WHICH ONE FETUS HAD AN OMPHALOCOELE

N. Nevin, M. Armstrong, 1975, British journal of obstetrics and gynaecology.

Periconceptional vitamin supplementation and the prevention of neural tube defects in south-east England and Northern Ireland.

M. Seller, N. Nevin, 1984, Journal of medical genetics.

Genetics and Preventive Medicine

N. Nevin, 1969, Royal Society of Health journal.

The prevalence of inherited neuromuscular disease in Northern Ireland

N. Nevin, V. Patterson, E. Hicks, 1996, Neuromuscular Disorders.

Genetic disorders.

N C Nevin, N. Nevin, David Adler, 1982, Clinics in obstetrics and gynaecology.

A syndrome of brachyphalangy, polydactyly and absent tibiae

R. Winter, C. Hall, M. Baraitser, 1997, Clinical dysmorphology.

Axial mesodermal dysplasia spectrum.

N. Nevin, S. Brown, F. Stewart, 1993, American journal of medical genetics.

Cystic hygroma simulating an encephalocele

N. Nevin, J. Nevin, W. Thompson, 1983, Prenatal diagnosis.

T cell receptor beta chain polymorphisms are associated with cystic fibrosis.

C. Graham, S. Mcmillan, N. Nevin, 1989, Journal of medical genetics.

First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.

P. Morrison, N. Nevin, R. Tubman, 2000, American journal of medical genetics.

Macha's curse: an Ulster pedigree

D. King, N. Nevin, R. Montgomery, 1992, Irish Journal of Psychological Medicine.

The KBG syndrome, characteristic dental findings: a case report.

M. King, N. Nevin, P. Fleming, 2008, International journal of paediatric dentistry.

Congenital heart disease in Down's syndrome: two year prospective early screening study.

B. Craig, M. Shields, N. Nevin, 1991, BMJ.

Cloacal defect in a 23-year-old with 47,XXX karyotype and clinical features of Cat Eye syndrome

N. Nevin, K. Johnston, J. W. Park, 2002, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Clinicopathological study of Refsum's disease with particular reference to fatal complications.

I. Allen, N. Nevin, D. McCormick, 1978, Journal of neurology, neurosurgery, and psychiatry.

reference to fatal complications . Refsum ' s disease with particular Clinicopathological study of

I. Allen, N. Nevin, D. McCormick, 2022 .

Refsum's syndrome. Heredopathia atactica polyneuritiformis.

J. Cumings, N. Nevin, F. McKeown, 1967, Brain : a journal of neurology.

The Association of Keratosis Pilaris Atrophicans with Hereditary Woolly Hair

N. Nevin, P. Mchenry, E. Bingham, 1990, Pediatric dermatology.

Letterer‐Siwe disease: a study of thirteen cases over a 21‐year period

N. Nevin, D. Burrows, A. Kelly, 1982, The British journal of dermatology.

CUTIS GYRATUM, ACANTHOSIS NIGRICANS AND OTHER CONGENITAL ANOMALIES A NEW SYNDROME

N. Ireland, N. Nevin, J. Dodge, 1969, The British journal of dermatology.

An 18 week fetus with Elejalde syndrome (acrocephalopolydactylyous dysplasia).

M. Armstrong, N. Nevin, B. Herron, 1994, Clinical dysmorphology.

De novo direct duplication 2 (p12 p21) with paternally inherited pericentric inversion 2p11.2 2q12.2

Michael A. Stewart, S. McKee, M. Humphreys, 1998, Clinical genetics.

Non-directive genetic counselling

M. Pembrey, P. Morrison, N. Nevin, 1991, The Lancet.

False positive results with immunoreactive trypsinogen screening for cystic fibrosis owing to trisomy 13.

N. Nevin, F. J. Priest, 1991, Journal of medical genetics.

Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance.

A. Harding, A. Harding, N. Nevin, 1990, Journal of medical genetics.

Congenital anomalies in twins in Northern Ireland. I: Anomalies in general and specific anomalies other than neural tube defects and of the cardiovascular system, 1974-1979.

N. Nevin, J. Little, 1989, Acta geneticae medicae et gemellologiae.

Oral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case report.

N. Nevin, W. Hutchinson, D. Kernohan, 1994, American journal of medical genetics.

Hypochondroplasia.

N. Nevin, J. Glasgow, P. S. Thomas, 1978, Archives of disease in childhood.

Growth impairment following irradiation in one of a pair of monozygotic twins.

F. S. Grebbell, N. Nevin, A. Lyons, 1973, Clinical radiology.

Renal transplantation between monozygotic twins discordant for unilateral renal agenesis.

J. Mcevoy, N. Nevin, 1973, The Ulster medical journal.

The epidemiology of Huntington's disease in Northern Ireland.

P. Morrison, N. Nevin, W. Johnston, 1995, Journal of medical genetics.

DNA analysis and recombination in X-linked retinitis pigmentosa

I. Craig, D. Archer, C. Graham, 1990, Eye.

Congenital malformations and anticonvulsant drugs.

N. Nevin, J. Millar, 1973, Lancet.

Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria.

A. Ward, N. Nevin, D. Burrows, 1993, Human molecular genetics.

Prevalence of gallstones in patients with erythropoietic protoporphyria in Northern Ireland

N. Nevin, D. Burrows, D. Todd, 1992 .

Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase.

P. Morrison, N. Nevin, J. Jones, 1990, Journal of medical genetics.

COMPUTER‐ASSISTED CRANIAL TOMOGRAPHY IN TUBEROUS SCLEROSIS

N. Nevin, 1980, Developmental medicine and child neurology.

Prof Norman Nevin - References

N. Nevin, 2017 .

Insurance Implications for Individuals with a High Risk of Breast and Ovarian Cancer in Europe

J. Chang-Claude, P. Møller, D. Eccles, 2002, Disease markers.

Hereditary macular degeneration in three generations.

N. Nevin, S. S. Johnston, J. Darragh, 1973, The British journal of ophthalmology.

Hereditary deafness associated with branchial fistulae and external ear malformations

N. Nevin, D. Wood, 1977, The Journal of Laryngology & Otology.

Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland

C. Graham, P. Morrison, N. Nevin, 1989, Human Genetics.

Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition.

A. Irvine, N. Nevin, V. Boston, 1996, American journal of medical genetics.

Radiological findings in mild forms of Morquio's disease (MPS 1V A)

N. Nevin, J. Nelson, P. S. Thomas, 1991, European Radiology.

Genetic linkage of familial expansile osteolysis to chromosome 18q.

J. Weber, R. Mollan, R. Wallace, 1994, Human molecular genetics.

Tympanic membrane grafting: Animal and tissue culture experiments

A. Kerr, N. Nevin, G. Smyth, 1971, The Journal of Laryngology & Otology.

Graves ' disease and Down ' s syndrome SUMMARY

N. Nevin, M. Graya, J. M. DUNLOPt, 2022 .

Severe mental retardation due to maternal phenylketonuria.

N. Nevin, N. A. Carson, 1982, The Ulster medical journal.

Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.

R. Snell, D. Shaw, P. Harper, 1993, Journal of medical genetics.

Congenital anomalies in twins in Northern Ireland. II: Neural tube defects, 1974-1979.

N. Nevin, J. Little, 1989, Acta geneticae medicae et gemellologiae.

Polydactyly in a carrier of the gene for the Meckel syndrome.

N. Nevin, J. Nelson, E. J. Hanna, 1994, American journal of medical genetics.

NEUROPATHOLOGICAL CHANGES IN THE WHITE MATTER FOLLOWING HEAD INJURY

N. Nevin, 1967, Journal of neuropathology and experimental neurology.

Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia

C. Patterson, C. Graham, J. Zschocke, 2000, Archives of disease in childhood.

Clomiphene and neural tube defects.

N. Nevin, J. Harley, 1976, The Ulster medical journal.

Gene probe analysis in an informative family with multiple endocrine neoplasia syndrome type 2A (MEN 2A). Improvement in carrier risk estimation.

L. Kennedy, P. Morrison, N. Nevin, 1991, The Quarterly journal of medicine.

Presymptomatic screening for MEN-2A

P. Morrison, N. Nevin, A. Hughes, 1991, The Lancet.

MEN 2A: update on the Northern Ireland and Australian family.

P. Morrison, N. Nevin, C. Russell, 1989, Henry Ford Hospital medical journal.

Ocular manifestations in patients and female relatives of families with the oculocerebrorenal syndrome of Lowe.

N. Nevin, S. S. Johnston, 1976, Birth defects original article series.

Vitamins During Pregnancy and Neural Tube Defects

M. Seller, N. Nevin, 1990 .

Prevention of neural-tube-defect recurrences

M. Seller, N. Nevin, 1990, The Lancet.

A child with a ring G chromosome (46,XX, Gr).

N. Nevin, W. Campbell, B. MacLaverty, 1971, Journal of medical genetics.

Frontonasal dysostosis in two successive generations.

A. Leonard, N. Nevin, B. Jones, 1999, American journal of medical genetics.

Neural tube defect recurrence after 'partial' vitamin supplementation.

A. Read, M. Seller, R. Harris, 1989, Journal of medical genetics.

A study on limb reduction defects in six European regions.

E. Garne, E. Calzolari, C. Stoll, 1996, Annales de genetique.

Report of the delegation of clinical geneticists to China, Spring 1986.

P. Harper, R. Harris, N. Nevin, 1987, Biology and society : the journal of the Eugenics Society.

Mutation characterization of CFTR gene in 206 Northern Irish CF families: Thirty mutations, including two novel, account for ∼︁94% of CF chromosomes

M. Macek, C. Graham, N. Nevin, 1996 .

Familial primary spontaneous pneumothorax consistent with true autosomal dominant inheritance.

P. Morrison, N. Nevin, R. Lowry, 1998, Thorax.

second family . phalanges ( Cooks syndrome ) : report of a Anonychia and absence / hypoplasia of distal

D. Eedy, N. Nevin, P. S. Thomas, 2022 .

Additional Glomangioma Families Link to Chromosome 1p: No Evidence for Genetic Heterogeneity

S. Orlow, D. Marchuk, M. Speer, 2001, Human Heredity.

Chorionic villus sampling for Down's syndrome

M. Armstrong, A. Magee, N. Nevin, 1991, The Lancet.

Von Hippel-Lindau disease: an important differential diagnosis of polycystic kidney disease.

N. Nevin, J. Jefferson, J. Keogh, 1997, Nephrology, Dialysis and Transplantation.

Allelic and locus heterogeneity in inherited venous malformations.

M C Speer, N C Nevin, J T Calvert, 1999, Human molecular genetics.

Chromosome Analysis before Birth and its Value in Genetic Counselling

M. Ferguson-Smith, N. Nevin, M. Ferguson-Smith, 1971, British medical journal.

Idiopathic multicentric osteolysis: report of two new cases and a review of the literature.

R. Mollan, N. Nevin, R. Barr, 1989, American journal of medical genetics.

Familial Camptodactyly with Taurinuria

D. W. Neill, L. Hurwitz, N. Nevin, 1966, Journal of medical genetics.

Down syndrome associated with a familial 14/21 translocation.

N. Nevin, W. Johnston, E. J. Hanna, 1981, Ulster medical journal.

An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis.

D. Hadden, A. Irvine, N. Nevin, 1996, Journal of medical genetics.

Influence of Social Class on the Risk of Recurrence of Anencephalus and Spina Bifida

N. Nevin, J. Merrett, W. Johnston, 1981, Developmental medicine and child neurology.

Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome?

N. Nevin, F. Stewart, C. Corkey, 1994, Clinical genetics.

Incidence of congenital rubella syndrome in 19 regions of Europe in 1980–1986

F. Bianchi, E. Calzolari, H. Dolk, 1989, European Journal of Epidemiology.

Linkage of epidermolysis bullosa simplex to keratin gene loci.

K. Mckenna, A. Hughes, N. Nevin, 1992, Journal of medical genetics.

A family study of spina bifida and anencephalus in Belfast, Northern Ireland (1964 to 1968).

N. Nevin, W. Johnston, 1980, Journal of medical genetics.

bifida . anencephaly and / or spina previous infant with either pregnancy in women with a Potato avoidance during

N. Nevin, J. Merrett, 2022 .

Outcome of pregnancy in a rubella outbreak in Northern Ireland 1978-1979.

N. Nevin, H. O'neill, J. Connolly, 1984, The Ulster medical journal.

Klinefelter syndrome and non-Hodgkin lymphoma.

C. Morris, M. Humphreys, N. Nevin, 1997, Cancer genetics and cytogenetics.

Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland

G. Karadima, M. Petersen, M. Mikkelsen, 2000, Occupational and environmental medicine.

Tissue culture of surgically prepared temporalis fascia.

A. Kerr, N. Nevin, A. P. Walby, 1982, Clinical otolaryngology and allied sciences.

Familial Craniosynostosis with Oral Anomalies

N. Nevin, J. Dodge, D. Kernohan, 1970, Developmental medicine and child neurology.

Letter to the Editor: Detection of Cystic Fibrosis Protein by Isoelectric Focusing of Serum

N. Nevin, G. B. Nevin, G. W. Tully, 1979, Pediatric Research.

Cystic fibrosis in Northern Ireland.

N. Nevin, A. Redmond, G. B. Nevin, 1979, Journal of medical genetics.

Congenital heart disease and urinary tract abnormalities in two siblings with DOOR syndrome.

A. Magee, N. Nevin, P. S. Thomas, 1994, Pediatric pathology.

Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndrome.

N. Nevin, P. S. Thomas, M. Reid, 1982, American journal of medical genetics.

Risk of recurrence after two children with central nervous system malformations in an area of high incidence.

N. Nevin, W. Johnston, 1980, Journal of medical genetics.

Frontonasal dysostosis in two successive generations

A. Leonard, N. Nevin, B. Jones, 1999 .

X-linked clinical anophthalmos. Localization of the gene to Xq27-Xq28.

C. Graham, N. Nevin, R. Redmond, 1991, Ophthalmic paediatrics and genetics.

Carrier estimations in Duchenne muscular dystrophy families in Northern Ireland using RFLP analysis.

C. Graham, N. Nevin, A. Hill, 1990, Journal of medical genetics.

Ankyloglossum superius syndrome.

N. Nevin, D. Kernohan, A. Ross, 1980, Oral surgery, oral medicine, and oral pathology.

Congenital extrahepatic biliary atresia in two brothers.

P. Froggatt, N. Nevin, M. Bell, 1969, Journal of medical genetics.

Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellites.

C. Graham, N. Nevin, J. Nevin, 1995, Journal of medical genetics.

Family Study of Congenital Hydrocephalus

N. Nevin, W. Johnston, C. Adams, 1982, Developmental medicine and child neurology.

A comparison of neural tube defects identified by two independent routine recording systems for congenital malformations in Northern Ireland.

N. Nevin, J. R. Mcdonald, A. L. Walby, 1978, International journal of epidemiology.

Trends in Prevalence of Congenital Abnormalities

N. Nevin, 1991 .

NEURAL TUBE DEFECTS

N. Nevin, P. Jongbloet, 1981, The Lancet.

Anencephalus and spina bifida in Belfast (1964-1968).

J. Elwood, N. Nevin, 1973, The Ulster medical journal.

A case of the orocraniodigital (Juberg-Hayward) syndrome.

N. Nevin, P. Henry, P. Thomas, 1981, Journal of medical genetics.

Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes

M. Tassabehji, C. Graham, N. Nevin, 1996, Human mutation.

Tumour necrosis factor microsatellites show association with multiple sclerosis

C. Graham, S. Mcmillan, S. Hawkins, 1997, Journal of the Neurological Sciences.

Facio-cardio-renal (Eastman-Bixler) syndrome.

A. E. Hill, N. Nevin, D. J. Carson, 1991, American journal of medical genetics.

Congenital Extrahepatic Biliary Atresia

P. Froggatt, N. Nevin, M. Bell, 2006 .

Two cases of trisomy D associated with adrenal tumours.

I. Allen, N. Nevin, J. Dodge, 1972, Journal of medical genetics.

Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.

P. Morrison, N. Nevin, J. Hughes, 2001, Ulster medical journal.

Periconceptional vitamin supplementation and the prevention of neural tube defects with an NTD undergoing amniocentesis during the period 1973 to 1981

M. Seller, N. Nevin, 2022 .

[The aglossia-adactylia syndrome].

N. Nevin, D. Burrows, D. Kernohan, 1976, Helvetica paediatrica acta.

Trisomy 20 mosaicism in amniotic fluid cell culture

N. Nevin, W. Thompson, J. Nevin, 1979, Clinical genetics.

From DNA to the Community

Maria do Rosário Silva, A. Kent, D. Gaudet, 2000, Public Health Genomics.

Laryngo-onycho-cutaneous syndrome associated with familial benign hypercalcemia.

N. Nevin, M. Walsh, J. Handley, 1993, Journal of the American Academy of Dermatology.

Hereditary benign telangiectasia--first family in Northern Ireland.

M. McMullin, N. Nevin, F. McNicholl, 1999, The Ulster medical journal.

Congenital familial dwarfism with cephalo-skeletal dysplasia.

N. Nevin, P. S. Thomas, 1976, Annales de radiologie.

Linkage data for Marfan syndrome and markers on chromosomes 1 and 11.

A. Child, A. Paepe, N. Nevin, 1990, Journal of medical genetics.

Wolcott‐Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11–12

M. Humphreys, C. Thornton, N. Nevin, 1996, Clinical genetics.

Detection of cystic fibrosis homozygotes and heterozygotes by serum isoelectrofocusing

N. Nevin, A. Redmond, G. B. Nevin, 1981, Human Genetics.

Fluorescent multiplex microsatellites used to identify haplotype associations with 15 CFTR mutations in 124 Northern Irish CF families

C. Graham, N. Nevin, D. Hughes, 1995, Human Genetics.

Hereditary breast cancer and linkage analysis to BRCA1

N. Nevin, S. Russell, R. A. J. Spence, 1995, British Journal of Surgery.

A NEW DYSPLASIA

J. Kanis, R. Mollan, J. Sloan, 1988 .

Dysgammaglobulinaemia complicated by disseminated measles.

D. W. Neill, I. Allen, M. Haire, 1971, British medical journal.

Prenatal diagnosis of Smith-Lemli-Opitz syndrome.

J. Dornan, N. Nevin, F. Stewart, 1995, American journal of medical genetics.

Norrie's disease.

N. Nevin, S. S. Johnston, J. Bryars, 1982, Birth defects original article series.

A Second Family with Probable CRAC (Colorectal Adenomata and Carcinoma) Syndrome—A New Familial Cancer

P. Morrison, N. Nevin, C. E. Chu, 2002, Disease Markers.

Two cases of trisomy D associated with adrenal tumours.

I. Allen, N. Nevin, J. Dodge, 1972, Journal of medical genetics.

PROLONGED COMA AFTER HEAD INJURY

N. Nevin, 1966 .

Letter: Raised alpha-fetoprotein levels and congenital defect.

N. Nevin, W. Thompson, G. Roberts, 1976, British medical journal.

Confidential inquiry into families with two siblings with cystic fibrosis

P. Morrison, A. Magee, N. Nevin, 1998, Archives of disease in childhood.

The epidemiology of Huntington's disease in Northern Ireland.

N. Nevin, W. Johnston, P. Morrison, 1995, Journal of medical genetics.

Huntington disease in County Donegal: epidemiological trends over four decades.

N. Nevin, P J Morrison, 1993, The Ulster medical journal.

An unusual case of chronic granulocytic leukaemia

N. Nevin, J. Bridges, A. Redmond, 1971, Irish journal of medical science.

Cleft lip and palate, hypertelorism, brachycephaly, flat facial profile, and congenital heart disease in three brothers.

B. Craig, F. Casey, N. Nevin, 1997, American journal of medical genetics.

Early amniocentesis: effect of removing a reduced volume of amniotic fluid on pregnancy outcome

N. Nevin, J. Nevin, S. Tharmaratnam, 1998, Prenatal diagnosis.

Isolated absence of IgA with autosomal dominant inheritance.

G. Tomkin, N. Nevin, N. Nevin, 1971, Lancet.