European approach to the human gene projectFERGUSON-SMITH, M. A.The FASEB journal. 1991, Vol 5, Num 1, pp 61-65, issn 0892-6638, 5 p.Article

Prenatal chromosome analysis and its impact on the birth incidence of chromosome disordersFERGUSON-SMITH, M. A.British medical bulletin. 1983, Vol 39, Num 4, pp 355-364, issn 0007-1420Article

The reduction of anencephalic and spina bifida births by maternal serum alphafetoprotein screeningFERGUSON-SMITH, M. A.British medical bulletin. 1983, Vol 39, Num 4, pp 365-372, issn 0007-1420Article

Invited editorial : putting the genetics back into cytogeneticsFERGUSON-SMITH, M. A.American journal of human genetics. 1991, Vol 48, Num 2, pp 179-182, issn 0002-9297Article

Early fetal diagnosis : recent progress and public health implication, Prague 8-14 July 1990FERGUSON-SMITH, M. A.Prenatal diagnosis. 1991, Vol 11, Num 8, pp 489-670, issn 0197-3851Conference Paper

Progress in the molecular cytogenetics of manFERGUSON-SMITH, M. A.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1988, Vol 319, Num 1194, pp 239-248, issn 0080-4622Conference Paper

Sex determination in mouse and man, discussion, London, 9-10 March 1988MCLAREN, A; FERGUSON-SMITH, M. A.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1988, Vol 322, Num 1208, pp 1-157, issn 0080-4622Conference Proceedings

Optimising human chromosome separation for the production of chromosome-specific DNA libraries by flow sortingHARRIS, P; BOYD, E; FERGUSON-SMITH, M. A et al.Human genetics. 1985, Vol 70, Num 1, pp 59-65, issn 0340-6717Article

Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52965 amniocentesesFERGUSON-SMITH, M. A; YATES, J. R. W.Prenatal diagnosis. 1984, Vol 4, pp 5-44, issn 0197-3851Article

Diagnosis of sex and cystic fibrosis status in fetal erythroblasts isolated from cord bloodGRIFFIN, D. K; FERGUSON-SMITH, M. A.Prenatal diagnosis. 1999, Vol 19, Num 2, pp 172-174, issn 0197-3851Article

Predictive value of amniotic acetylcholinesterase analysis in the diagnosis of fetal abnormality in 3700 pregnanciesAITKEN, D. A; MORRISON, N. M; FERGUSON-SMITH, M. A et al.Prenatal diagnosis. 1984, Vol 4, Num 5, pp 329-340, issn 0197-3851Article

Microvillar enzyme analysis in amniotic fluid and the prenatal diagnosis of cystic fibrosisAITKEN, D. A; YAQOOB, M; FERGUSON-SMITH, M. A et al.Prenatal diagnosis. 1985, Vol 5, Num 2, pp 119-127, issn 0197-3851Article

Placental haemangioma. Case reportMANN, L; ALROOMI, L; MCNAY, M et al.British journal of obstetrics and gynaecology (Print). 1983, Vol 90, Num 10, pp 983-986, issn 0306-5456Article

Toward a multicolor chromosome bar code for the entire human karyotype by fluorescence in situ hybridizationMÜLLER, S; ROCCHI, M; FERGUSON-SMITH, M. A et al.Human genetics. 1997, Vol 100, Num 2, pp 271-278, issn 0340-6717Article

Comparative genomics : tracking chromosome evolution in the family Ursidae using reciprocal chromosome paintingNASH, W. G; WIENBERG, J; FERGUSON-SMITH, M. A et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 3-4, pp 182-192, issn 0301-0171Conference Paper

Conservation of human vs. feline genome organization revealed by reciprocal chromosome paintingWIENBERG, J; STANYON, R; NASH, W. G et al.Cytogenetics and cell genetics. 1997, Vol 77, Num 3-4, pp 211-217, issn 0301-0171Article

Use of the Indian muntjac idiogram to align conserved chromosomal segments in sheep and human genomes by chromosome paintingBURKIN, D. J; YANG, F; BROAD, T. E et al.Genomics (San Diego, Calif.). 1997, Vol 46, Num 1, pp 143-147, issn 0888-7543Article

Reciprocal chromosome painting between human and prosimians (Eulemurmacaco macaco and E. fulvus mayottensis)MÜLLER, S; O'BRIEN, P. C. M; FERGUSON-SMITH, M. A et al.Cytogenetics and cell genetics. 1997, Vol 78, Num 3-4, pp 260-271, issn 0301-0171Conference Paper

A method for creating chromosome-specific plasmid libraries enriched in clones containing [CA]_n microsatellite repeat sequences directly from flow-sorted chromosomesLYALL, J. E. W; BROWN, G. M; FURLONG, R. A et al.Nucleic acids research. 1993, Vol 21, Num 19, pp 4641-4642, issn 0305-1048Article

Gender verification in competitive sportsSIMPSON, J. L; LJUNGQVIST, A; DE LA CHAPELLE, A et al.Sports medicine (Auckland). 1993, Vol 16, Num 5, pp 305-315, issn 0112-1642Article

Prenatal diagnosis from maternal blood : simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sortingYUN-LING ZHENG; CARTER, N. P; PRICE, C. M et al.Journal of medical genetics. 1993, Vol 30, Num 12, pp 1051-1056, issn 0022-2593Article

Cytogenetic and molecular investigation of an abnormal Y chromosome : evidence for a pseudo-dicentric (Yq) isochromosomeSAVARY, J. B; VASSEUR, F; FLACTIF, M et al.Annales de génétique (Paris). 1992, Vol 35, Num 3, pp 134-139, issn 0003-3995Article

Abnormalities of human sex determinationFERGUSON-SMITH, M. A.Journal of inherited metabolic disease. 1992, Vol 15, Num 4, pp 518-525, issn 0141-8955Conference Paper

A consortium approach to molecular genetic servicesBROCK, D. J. H; JOHNSTON, A. W; BARRON, L et al.Journal of medical genetics. 1990, Vol 27, Num 1, pp 8-13, issn 0022-2593, 6 p.Article

Genotype-phenotype correlations in XX males and their bearing on current theories of sex determinationFERGUSON-SMITH, M. A; COOKE, A; AFFARA, N. A et al.Human genetics. 1990, Vol 84, Num 2, pp 198-202, issn 0340-6717, 5 p.Article