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Clinical Genetics|April 1, 1995
Familial hypertryptophanemia in two siblingsJ R Martin, C S Mellor, F C FraserAmerican Journal of Medical Genetics|March 1, 1983
Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome?F C Fraser, S Aymé, F Halal, et al.American Journal of Medical Genetics|January 1, 1978
Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomaliesF C Fraser, D Ling, D Clogg, et al.Clinical Genetics|February 1, 1986
A simple technique for recording and counting sweat pores on the dermal ridgesE O'Leary, J Slaney, D G Bryant, et al.American Journal of Medical Genetics|December 31, 1997
Poland sequence with dextrocardia: which comes first?F C Fraser, A S Teebi, S Walsh, et al.Journal of the Neurological Sciences|July 1, 1987
The clinical consequences of X-chromosome inactivation: Duchenne muscular dystrophy in one of monozygotic twinsS D Pena, G Karpati, S Carpenter, et al.Clinical Genetics|August 1, 1996
Multifactorial inheritance of non-syndromic macrocephalyL Arbour, G V Watters, J G Hall, et al.Clinical Genetics|July 1, 1987
An aminopterin-like syndrome without aminopterin (ASSAS)F C Fraser, R A Anderson, J I Mulvihill, et al.Science (New York, N.Y.)|May 26, 1978
Genetics and Medicine: an evolving relationshipC R Scriver, C Laberge, C L Clow, et al.Journal of Medical Genetics|December 1, 1977
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangyA G Hunter, P J McAlpine, N L Rudd, et al.Pageof 8