J. M. Connor

发表

Malcolm A. Ferguson-Smith, M. Niermeijer, J. M. Connor, 1997, Annals of Internal Medicine.

M. Ferguson-Smith, M. A. Ferguson-Smith, J. M. Connor, 1987 .

Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant.

M. McNay, J. M. Connor, R. Connor, 1985, American journal of medical genetics.

Quantitative and qualitative studies on skin fibroblast alkaline phosphatase in fibrodysplasia ossificans progressiva.

D. Evans, J. M. Connor, 1981, Clinica chimica acta; international journal of clinical chemistry.

Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1).

D. Kwiatkowski, M. Nellist, J. Sampson, 1993, Journal of medical genetics.

Conclusions and Clinical Implications

J. M. Connor, 1983 .

Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients.

D. Evans, J. M. Connor, 1982, The Journal of bone and joint surgery. British volume.

Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry.

J. Tolmie, J. M. Connor, E. Boyd, 1989, American journal of medical genetics.

Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformity.

J. Tolmie, J. M. Connor, J. Tolmie, 1988, The Journal of bone and joint surgery. British volume.

Genetic aspects of early childhood scoliosis.

J. Tolmie, D. Goudie, J. M. Connor, 1987, American journal of medical genetics.

Genetic heterogeneity in tuberous sclerosis: phenotypic correlations.

P. Beighton, I. Winship, J. M. Connor, 1990, Journal of medical genetics.

Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland.

C. Forbes, G. Lowe, N. Affara, 1985, Journal of medical genetics.

Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.

C. Forbes, G. Lowe, I. Hann, 1986, Journal of medical genetics.

Diagnosis in Prader-Willi syndrome.

J. Tolmie, W. Parry-Jones, J. M. Connor, 1994, Archives of disease in childhood.

Possible role of imprinting in the Turner phenotype.

S. Greene, J. M. Connor, M. Donaldson, 1994, Journal of medical genetics.

Paediatric podiatry and genetics

J. M. Connor, D. Wilcox, D. Goel, 2006 .

Ossification After Major Trauma

J. M. Connor, 1983 .

Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

J. Yates, J. M. Connor, J. Crossley, 1987, Journal of medical genetics.

Experimental Production of Ectopic Bone

J. M. Connor, 1983 .

International Directory of Genetic Services

J M Connor, J. M. Connor, 1991 .

Dyskeratosis congenita. Report of a large kindred

J. Connor, J. M. Connor, R. Teague, 1981, The British journal of dermatology.

Bilateral posterior scleral ossification.

W. Green, J. Patrinely, J. M. Connor, 1982, American journal of ophthalmology.

Genetic aspects of tuberous sclerosis in the west of Scotland.

J B Stephenson, J. Sampson, J. Stephenson, 1989, Journal of medical genetics.

Molecular biology of Turner's syndrome.

J. M. Connor, C. E. Chu, C E Chu, 1995, Archives of disease in childhood.

Molecular Genetics of Turner's Syndrome

J. M. Connor, S. Loughlin, S.A.R. LOUGHLIN, 1989, Acta paediatrica Scandinavica. Supplement.

Detection of Y mosaicism in patients with Turner's syndrome.

S. Greene, J. M. Connor, M. Donaldson, 1995, Journal of medical genetics.

Prenatal diagnosis in obstetric practice

M. Whittle, J. M. Connor, 1989 .

Non‐dermatological complications and genetic aspects of the Rothmund‐Thomson syndrome

J. Mcclure, J. M. Connor, D. Starr, 1985, Clinical genetics.

Second trimester prenatal diagnosis of the Jarcho‐Levin syndrome

J. Tolmie, M. McNay, M. Whittle, 1987, Prenatal diagnosis.

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

S. Povey, J. M. Connor, A. Fryer, 1987, The Lancet.

An analysis of the parental age effect for inv dup (15).

D. Gilmore, J. M. Connor, 1984, Journal of medical genetics.

Screening for genetic abnormality

J. M. Connor, 1989 .

Soft Tissue Ossification

J. M. Connor, 1983 .

Fibrodysplasia ossificans progressiva in South Africa. Case reports.

P. Beighton, J. M. Connor, 1982, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

The radiological spectrum of fibrodysplasia ossificans progressiva.

P. Beighton, J. M. Connor, B. Cremin, 1982, Clinical Radiology.

Thrombocytopenia with absent radii (TAR) syndrome: a new increased cellular radiosensitivity syndrome.

P. Bryant, N. Liu, B. J. Clark, 1995, Clinical oncology (Royal College of Radiologists (Great Britain)).

Concordant monozygotic twins with bilateral renal agenesis.

J. M. Connor, J. Yates, J. Duke, 1984, Journal of medical genetics.

Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child.

J. Tolmie, M. McNay, J. M. Connor, 1987, American journal of medical genetics.

Monozygous twins concordant for duodenojejunal villous atrophy and dermatitis herpetiformis.

S. Green, J. M. Connor, S. Natarajan, 1986, Gut.

Recent Linkage Studies in Tuberous Sclerosis

J. Sampson, J. M. Connor, 1991 .

Dominant inheritance of Scheuermann's juvenile kyphosis.

J. M. Connor, A. N. Conner, A. Findlay, 1989, Journal of medical genetics.

Other Causes of Soft Tissue Ossification

J. M. Connor, 1983 .

Evidence for genetic heterogeneity in tuberous sclerosis.

P. Beighton, J. Sampson, J. Yates, 1989, Journal of medical genetics.

Pycnodysostosis in a Pakistani Family: Case Presentation and Review

J. M. Connor, K. Goel, Alison M. Kerr, 1985, Scottish medical journal.

the west of Scotland . counselling for haemophilia B in genomic probe to genetic Application of an intragenic

C. Forbes, I. Hann, J. M. Connor, 2022 .

An increased incidence of thyroid antibodies in patients with Turner's syndrome and their first degree relatives.

J. Mckillop, J. Thomson, J. M. Connor, 1996, Autoimmunity.

23 Genetic Analysis

J. M. Connor, 1991 .

Cloning of the gene for the fragile X syndrome: implications for the clinical geneticist.

J. M. Connor, 1991, Journal of medical genetics.

Medical Genetics for the MRCOG and Beyond

E. Tobias, J. M. Connor, 2005 .

Genetic aspects of prenatal diagnosis

J. M. Connor, 1989, Journal of Inherited Metabolic Disease.

A three generation family with fibrodysplasia ossificans progressiva.

H. Skirton, J. M. Connor, P. Lunt, 1993, Journal of medical genetics.

Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset a

J. Haines, M. Pericak-Vance, J. Attwood, 1991, Annals of the New York Academy of Sciences.

Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl.

M. Ferguson-Smith, J. Yates, J. M. Connor, 1987, Journal of medical genetics.

Multiple odontogenic keratocysts in a case of the Noonan syndrome.

D. Evans, J. M. Connor, D. H. Goose, 1982, The British journal of oral surgery.

Differentiation between cleft palate and cleft lip and palate using genotypic markers

P. Mossey, J. M. Connor, J. McColl, 1996 .

Ossification in Neurological Conditions

J. M. Connor, 1983 .

Differential Diagnosis of Soft Tissue Calcification

J. M. Connor, 1983 .

Genetic linkage.

J. Yates, J. M. Connor, 1986, British journal of hospital medicine.

Molecular Basis of Inherited Disease

J. M. Connor, 1993 .

Mucosal neuroma syndrome--a phenotype for malignancy.

J. M. Connor, K. Goel, M. White, 1985, Archives of disease in childhood.

Genetic causes of mental handicap and opportunities for prevention.

M. Ferguson-Smith, J. M. Connor, 1988, Bailliere's clinical obstetrics and gynaecology.

Genetics of mental handicap

J. M. Connor, 1993 .

Syndrome of the month

J. M. Connor, H. R. Davidson, D. Guthrie, 2022 .

The phenotype of fibrodysplasia ossificans progressiva

J. Connor, F. Kaplan, D. Glaser, 2005 .

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, llq, and 12q

M. Pericak-Vance, Cardiff, S. Povey, 2022 .

FIRST TRIMESTER PRENATAL EXCLUSION OF TUBEROUS SCLEROSIS

M. Whittle, J. M. Connor, S. Loughlin, 1987, The Lancet.

Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers.

J. Yates, J. Stephenson, J. M. Connor, 1987, Cytogenetics and cell genetics.

NON-PENETRANCE IN TUBEROUS SCLEROSIS

J. M. Connor, M. Hadley, J. Stephenson, 1986, The Lancet.

Genetic linkage.

J. M. Connor, J. Yates, 1986, British journal of hospital medicine.

Clinical Molecular Genetics

J. M. Connor, 1993 .