M. Faed

发表

Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).

J. S. Beck, M. Faed, J. Robertson, 1987, Journal of medical genetics.

Ascertainment and severity of Marfan syndrome in a Scottish population.

T. Pringle, P. Baines, J. Dean, 1994, Journal of medical genetics.

A cytogenetic survey of men being investigated for subfertility.

M. Faed, J. Robertson, K. Baxby, 1979, Journal of reproduction and fertility.

Comparative studies of spermatogenesis in fertile and subfertile men.

M. Faed, K. Baxby, M. Lamont, 1981, Journal of clinical pathology.

Paris Conference (1971): Standardization in human cytogenetics.

J. F. Lasley, B. N. Day, H. Klinger, 1972, Cytogenetics.

Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man

P. Batstone, R. Speed, M. Faed, 1991, Human Genetics.

HLA antigens in a Scottish psoriatic population.

I. Gunn, T. Lakshmipathi, M. Faed, 2008, Tissue antigens.

The frequency of constitutional chromosome abnormalities in patients with malignant disease.

D. Harnden, M. Faed, S. McBeath, 1969, European journal of cancer.

Enhancement by caffeine of sister-chromatid exchange frequency in lymphocytes from normal subjects after treatment by mutagens.

D. Mourelatos, M. Faed, 1978, Mutation research.

A chromosome survey of a hospital for the mentally subnormal

M. Faed, J. Mellon, I. Robertson, 1979, Clinical genetics.

Pericentric inversion of a group C autosome: a study of three families

P. Jacobs, H. Harris, E. Robson, 1968, Annals of human genetics.

Books received for review

J. F. Lasley, B. N. Day, H. Klinger, 1923, The Mathematical Gazette.

Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly.

M. Faed, K. Baxby, M. Lamont, 1982, Journal of medical genetics.

Spermatogenesis in an infertile XYY man

M. Faed, J. Robertson, J. Grieve, 1976, Human Genetics.

Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception

J. Mills, R. Mahmood, J. Delhanty, 2000, Human Genetics.

Nucleolus organiser regions on mitotic and meiotic chromosomes from infertile males investigated using a specific silver stain

J. Ironside, M. Faed, 1979, Human Genetics.

Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern.

M. Faed, J. Robertson, M. Lamont, 1982, Journal of medical genetics.

Prenatal exclusion testing for Huntington's disease: a problem of too much information.

A. Curtis, M. Boxer, D. Brock, 1989, Journal of medical genetics.

Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers

M. Faed, J. Robertson, J. Wolstenholme, 2004, Human Genetics.

Wiedemann-Beckwith syndrome in one of monozygotic twins.

M. Faed, B. Bose, M. Madlom, 1986, Archives of disease in childhood.

A female with the 48,XXXX karyotype.

M. Faed, M. Berkeley, 1970, Journal of medical genetics.

Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings

A. Carothers, G. Lowther, P. M. Ellis, 1999, Genetic epidemiology.

An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9

M. Faed, J. Robertson, M. Lamont, 1978, Clinical genetics.

47, XYY chromosome constitution, physical growth and psychological disturbance. A case study.

M. Faed, M. Field, 1974, Journal of child psychology and psychiatry, and allied disciplines.

Incidence of familial Hodgkin's disease.

P. Smith, L. Kerzin-Storrar, M. Faed, 1983, British Journal of Cancer.

Trisomy 21 in transient myeloproliferative disorder.

W. Tarnow-Mordi, M. Faed, J. Robertson, 1990, Cancer genetics and cytogenetics.

Pure partial trisomy for long arm of chromosome 9.

P. Smail, S. Brown, M. Faed, 1976, Journal of medical genetics.

Marfan syndrome in a large family: response of family members to a screening programme.

C. Bundy, J. Gray, M. Boxer, 1992, Journal of medical genetics.

Marfan syndrome affecting four generations of a family without ocular involvement.

T. Pringle, G. Mcneill, M. Boxer, 1991, Postgraduate medical journal.

Comparative genomic hybridization analysis of human oocytes and polar bodies.

A. Thornhill, J. Harper, D. Wells, 2006, Human reproduction.

Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.

C. Paterson, M. Faed, J. Robertson, 1972, Journal of medical genetics.

Integrity of the telomere.

M. Faed, J. Robertson, 1972, Lancet.

Sister chromatid exchange frequency in human epidermal cells in culture treated with 8-methoxypsoralen and long-wave UV radiation.

M. R. West, M. Faed, M. Johansen, 1982, The Journal of investigative dermatology.

Chromosome abnormalities in two cases with bilateral radial element defects.

A. Stewart, M. Faed, A. Keay, 1969, Journal of medical genetics.

Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.

E. Robson, P. Cook, M. Faed, 1973, Cytogenetics.

Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease.

M. Faed, J. Robertson, H. G. Morton, 1972, Journal of medical genetics.

Improved fragile site detection with trimethoprim

D. McLean, M. Faed, 1990, Human Genetics.

45,X/46,X dic (Y) mosaicism in a phenotypic male.

J. Gosden, P. Batstone, M. Faed, 1991, Archives of Disease in Childhood.

Sister chromatid exchanges in human lymphocytes exposed to 8-methoxypsoralen and long wave UV radiation prior to incorporation of bromodeoxyuridine

D. Mourelatos, B. Johnson, M. Faed, 1977, Experientia.

Sister chromatid exchanges in lymphocytes of psoriatics after treatment with 8‐methoxypsoralen and long wave ultraviolet radiation

W. Frain-Bell, D. Mourelatos, P. Gould, 1977, The British journal of dermatology.

Screening for Down's syndrome based on individual risk.

P. Howie, M. Faed, M. Lewis, 1991, BMJ.

Cytogenetic andhistological studies oftesticular biopsies fromsubfertile men withchromosome anomaly

M. Faed, M. Lamont, 1982 .

Proceedings: Gaucher's disease with biclonal gammopathy.

A. J. Wood, G. R. Tudhope, P. Mitchell, 1975, Journal of clinical pathology.

Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms

J. Delhanty, S. Cupisti, E. Fragouli, 2003, Prenatal diagnosis.

Pseudohermaphroditism due to XY gonadal absence syndrome*

P. Smail, M. Sinclair, M. Faed, 2022 .

THE FETAL MANIFESTATIONS OF THE 45XO KARYOTYPE

D. Rushton, M. Faed, A. Bain, 1969, The Journal of obstetrics and gynaecology of the British Commonwealth.

Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatment

W. Frain-Bell, B. Johnson, T. Lakshmipathi, 1980, The British journal of dermatology.

Marfan syndrome in a large family: response of family members to a screening programme.

C. Bundy, J. Gray, A. Bridges, 1992, Journal of medical genetics.

Pseudohermaphroditism due to XY gonadal absence syndrome*

P. Smail, M. Sinclair, M. Faed, 2022 .

Effect of 8-methoxypsoralen in the dark on sister-chromatid exchange frequency in human lymphocytes.

M. Faed, S. Peterson, 1980, Mutation research.