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Human Genetics|July 1, 1992
Three DNA markers for hypophosphataemic ricketsP S Rowe, A P Read, R Mountford, et al.Genes, Chromosomes & Cancer|December 31, 1997
Deletion mapping defines three discrete areas of allelic imbalance on chromosome arm 8p in oral and oropharyngeal squamous cell carcinomasC L Wu, L Roz, P Sloan, et al.International Journal of Epidemiology|November 1, 2011
Apparent prevention of neural tube defects by periconceptional vitamin supplementation. 1981R W Smithells, S Sheppard, C J Schorah, et al.Journal of Medical Genetics|February 1, 1994
Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family registerR G Elles, K A Hodgkinson, N P Mallick, et al.Archives of Disease in Childhood|December 1, 1981
Apparent prevention of neural tube defects by periconceptional vitamin supplementationR W Smithells, S Sheppard, C J Schorah, et al.Lancet (London, England)|February 16, 1980
Possible prevention of neural-tube defects by periconceptional vitamin supplementationR W Smithells, S Sheppard, C J Schorah, et al.American Journal of Human Genetics|January 23, 1999
Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypesM Tassabehji, K Metcalfe, A Karmiloff-Smith, et al.Human Molecular Genetics|January 1, 1996
Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175K A Brown, A H Janjua, G Karbani, et al.The Journal of Laryngology and Otology|January 1, 1993
A clinical, genetic and audiological study of patients and families with bilateral acoustic neurofibromatosisW J Neary, V E Newton, M Vidler, et al.Human Molecular Genetics|August 11, 1999
A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathiesN Bondurand, K Kuhlbrodt, V Pingault, et al.Pageof 10