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Journal of Medical Genetics|July 1, 1990
Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?R G Elles, A P Read, K A Hodgkinson, et al.Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.Journal of Medical Genetics|December 10, 2002
Comparison of genetic services with and without genetic registers: knowledge, adjustment, and attitudes about genetic counselling among probands referred to three genetic clinicsC Wright, L Kerzin-Storrar, P R Williamson, et al.Journal of Medical Genetics|July 1, 1987
Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4C McKeown, A P Read, A Dodge, et al.The British Journal of Ophthalmology|August 1, 1997
Anterior segment dysgenesis in mosaic Turner syndromeI C Lloyd, P M Haigh, J Clayton-Smith, et al.Brain : a Journal of Neurology|November 10, 2001
Abnormal corticospinal function but normal axonal guidance in human L1CAM mutationsC B Dobson, F Villagra, G J Clowry, et al.Journal of Medical Genetics|December 24, 1998
Costello syndrome: two cases with embryonal rhabdomyosarcomaB Kerr, O B Eden, R Dandamudi, et al.Journal of Medical Genetics|December 1, 1986
A register based system for gene tracking in Duchenne muscular dystrophyA P Read, L Kerzin-Storrar, R C Mountford, et al.Ophthalmology|May 18, 1999
A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophyH Stewart, G C Black, D Donnai, et al.Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.Pageof 19