M. Ferguson‐Smith

发表

A. Monaco, S. Warren, J. Schepens, 2011, Nucleic Acids Research.

A molecular deletion map of the Y chromosome long arm defining X and autosomal homologous regions and the localisation of the HYA locus to the proximal region of the Yq euchromatin.

E. Simpson, P. Chandler, N. Affara, 1992, Human molecular genetics.

Invited Editorial: Putting the Genetics Back into Cytogenetics

M. Ferguson‐Smith, 2006 .

Mapping the H-Y gene.

D. Page, C. Disteche, E. Simpson, 1987, Development.

Estimating the risk of a fetal autosomal trisomy at mid‐trimester using maternal serum alpha fetoprotein and age: A retrospective study of 142 pregnancies

J. Yates, J. Crossley, D. Aitken, 1991, Prenatal diagnosis.

The use of genetic linkage in counselling families with dystrophia myotonica

M. Ferguson‐Smith, S. Gibson, M. A. Ferguson-Smith, 1980, Clinical genetics.

A Gene Catalogue of the Euchromatic Male-Specific Region of the Horse Y Chromosome: Comparison with Human and Other Mammals

W. Murphy, B. Chowdhary, T. Raudsepp, 2011, PloS one.

Microvillar enzyme analysis in amniotic fluid and the prenatal diagnosis of cystic fibrosis

M. Yaqoob, D. Aitken, M. Ferguson‐Smith, 1985, Prenatal diagnosis.

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.

A. Bergen, A. Gal, C. Samanns, 1990, Ophthalmic paediatrics and genetics.

Down's syndrome due to maternal mosaicism, and the value of antenatal diagnosis.

R. Gadd, J. Timson, M. Ferguson‐Smith, 1971, Lancet.

Chromosomal localization of a single copy gene by in situ hybridization ‐ human β globin genes on the short arm of chromosome 11

M. Ferguson-Smith, S. Malcolm, P. Barton, 1981, Annals of human genetics.

The association of satellited chromosomes with specific chromosomal regions in cultured human somatic cells

M. Ferguson‐Smith, S. Handmaker, M. A. Ferguson-Smith, 1963, Annals of human genetics.

Prenatal assessment of anterior abdominal wall defects and their prognosis

A. Gibson, P. Raine, M. Ferguson‐Smith, 1984, Prenatal diagnosis.

Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses

J. Yates, M. Ferguson‐Smith, M. A. Ferguson-Smith, 1984, Prenatal diagnosis.

A SEMI‐AUTOMATED SERUM ALPHAFETOPROTEIN RADIOIMMUNOASSAY FOR PRENATAL SPINA BIFIDA SCREENING

T. J. Mcmanus, M. Ferguson‐Smith, J. Ratcliffe, 1975, British journal of obstetrics and gynaecology.

Second‐trimester maternal serum screening using alpha‐fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: Experience of a regional programme

S. Goodburn, J. Yates, M. Ferguson‐Smith, 1994, Prenatal diagnosis.

Amniotic fluid alpha‐fetoprotein, gamma‐glutamyltranspeptidase, and autosomal trisomies

M. Ferguson-Smith, G. Graham, J. Crossley, 1989, Prenatal diagnosis.

Predictive value of amniotic acetylcholinesterase analysis in the diagnosis of fetal abnormality in 3700 pregnancies

D. Aitken, M. Ferguson‐Smith, N. M. Morrison, 1984, Prenatal diagnosis.

Physical mapping of chromosome 3p25-p26 by flourescence in situ hybridisation (FISH)

Y. Nakamura, M. Lerman, B. Zbar, 1993, Human Genetics.

Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study

D. Spathas, M. Ferguson‐Smith, G. Maniatis, 1994, Prenatal diagnosis.

Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots.

N. Carter, M. Ferguson-Smith, N. Affara, 1990, Cytometry.

Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolution.

M. Leversha, M. Jackson, H. Thiesen, 1993, Nucleic acids research.

Normal development in two six‐year‐old boys born after prenatal diagnosis of trisomy 20 mosaicism

D. Gilmore, M. Ferguson‐Smith, M. Ferguson-Smith, 1987, Prenatal diagnosis.

Gene diagnosis in X-linked ichthyosis

B. Wirth, T. Kruse, K. Wulff, 2004, Archives of Dermatological Research.

Antenatal diagnosis of propianicacidaemia.

D. Gompertz, P. Goodey, M. Ferguson‐Smith, 1973, Lancet.

The linkage relationships of marker sites on chromosomes no. 2 and 10

J. German, R. Chaganti, L. Weitkamp, 1978, Annals of human genetics.

MATERNAL SERUM ALPHA‐FETOPROTEIN SCREENING FOR OPEN NEURAL TUBE DEFECTS IN TWIN PREGNANCIES

B. No̸rgaard-Pedersen, N. Wald, H. Cuckle, 1990, Prenatal diagnosis.

Prognostic significance of raised serum α‐fetoprotein levels in twin pregnancies

A. Ghosh, M. Ferguson‐Smith, H. Rawlinson, 1982 .

Detection by ultrasound of abnormality in twin pregnancies during the second trimester

J. Neilson, A. Gibson, M. Ferguson‐Smith, 1982, British Journal of Obstetrics and Gynaecology.

HETEROKARYOTYPIC MONOZYGOTIC TWINS AND THE ACARDIAC MONSTER

M. Ferguson‐Smith, J. Scott, M. A. Ferguson-Smith, 1973, The Journal of obstetrics and gynaecology of the British Commonwealth.

Localization of the retinoid X receptor alpha gene (RXRA) to chromosome 9q34

S. Povey, K. Woodward, J. Fitzgibbon, 1993, Annals of human genetics.

Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)

B. Wirth, M. Ferguson-Smith, K. Figura, 1988, Human Genetics.

The secretor status of the foetus

M. Ferguson‐Smith, Sheila L. M. Gibson, M. A. Ferguson-Smith, 1980, Clinical genetics.

MANAGEMENT OF CONGENITAL ADRENAL HYPERPLASIA

P. Betts, G. Beastall, P. Wood, 1984, The Lancet.