Malcolm A. Ferguson-Smith
Malcolm A. Ferguson-Smith
Emeritus Professor of Pathology, Cambridge University
Verified email at - Homepage
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Identification of the von Hippel-Lindau disease tumor suppressor gene
F Latif, K Tory, J Gnarra, M Yao, FM Duh, ML Orcutt, T Stackhouse, ...
Science 260 (5112), 1317-1320, 1993
Multicolor spectral karyotyping of human chromosomes
E Schröck, S Du Manoir, T Veldman, B Schoell, J Wienberg, ...
Science 273 (5274), 494-497, 1996
Clinical features and natural history of von Hippel-Lindau disease
ER Maher, JRW Yates, R Harries, C Benjamin, R Harris, AT Moore, ...
QJM: An International Journal of Medicine 77 (2), 1151-1163, 1990
Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia
CR Bartram, A de Klein, A Hagemeijer, T van Agthoven, AG van Kessel, ...
Nature 306 (5940), 277-280, 1983
Genome analysis of the platypus reveals unique signatures of evolution
Nature 453 (7192), 175-183, 2008
Cytogenetic analysis by chromosome painting using DOP‐PCR amplified flow‐sorted chromosomes
HÅK Telenius, BAJ Ponder, A Tunnacliffe, AH Pelmear, NP Carter, ...
Genes, Chromosomes and Cancer 4 (3), 257-263, 1992
Von Hippel-Lindau disease: a genetic study.
ER Maher, L Iselius, JR Yates, M Littler, C Benjamin, R Harris, J Sampson, ...
Journal of medical genetics 28 (7), 443-447, 1991
Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations
MA Ferguson-Smith
Journal of Medical Genetics 2 (2), 142, 1965
Germline mutations in the Von Hippel‐Lindau disease (VHL) gene in families from North America, Europe, and Japan
B Zbar, T Kishida, F Chen, L Schmidt, ER Maher, FM Richards, ...
Human mutation 8 (4), 348-357, 1996
Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses
MA Ferguson‐Smith, JRW Yates
Prenatal diagnosis 4 (7), 5-44, 1984
XY chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome
MA Ferguson-Smith
The Lancet 288 (7461), 475-476, 1966
Somatic mutations of the von Hippel—Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma
K Foster, A Prowse, A van den Berg, S Fleming, MMF Hulsbeek, ...
Human molecular genetics 3 (12), 2169-2173, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype.
PA Crossey, FM Richards, K Foster, JS Green, A Prowse, F Latif, ...
Human Molecular Genetics 3 (8), 1303-1308, 1994
Microsatellite evolution—evidence for directionality and variation in rate between species
DC Rubinsztein, W Amos, J Leggo, S Goodburn, S Jain, SH Li, ...
Nature genetics 10 (3), 337-343, 1995
A complete comparative chromosome map for the dog, red fox, and human and its integration with canine genetic maps
F Yang, PCM O'brien, BS Milne, AS Graphodatsky, N Solanky, V Trifonov, ...
Genomics 62 (2), 189-202, 1999
Observations on the satellited human chromosomes
MA Ferguson-Smith, SD Handmaker, ABJ Hopkins
The Lancet 277 (7178), 638-640, 1961
Bird-like sex chromosomes of platypus imply recent origin of mammal sex chromosomes
F Veyrunes, PD Waters, P Miethke, W Rens, D McMillan, AE Alsop, ...
Genome research 18 (6), 965-973, 2008
Multicolour spectral karyotyping of mouse chromosomes
M Liyanage, A Coleman, S Manoir, T Veldman, S McCormack, ...
Nature genetics 14 (3), 312-315, 1996
Mammalian karyotype evolution
MA Ferguson-Smith, V Trifonov
Nature Reviews Genetics 8 (12), 950-962, 2007
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
A Ballabio, B Bardoni, R Carrozzo, G Andria, D Bick, L Campbell, ...
Proceedings of the National Academy of Sciences 86 (24), 10001-10005, 1989
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