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Journal of Medical Genetics|January 1, 1996
Clinical features of cystic fibrosis patients with rare genotypesG Castaldo, E Rippa, V Raia, et al.Journal of Medical Genetics|December 1, 1995
X inactivation of the FMR1 fragile X mental retardation geneC U Kirchgessner, S T Warren, H F WillardJournal of Medical Genetics|December 1, 1995
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomasC Eng, P A Crossey, L M Mulligan, et al.Journal of Medical Genetics|December 1, 1995
Ophthalmic genetics: a genealogical guide to sources in England and WalesM JayJournal of Medical Genetics|December 1, 1995
Cytogenetic and molecular findings in patients with Turner's syndrome stigmataT Kuznetzova, A Baranov, N Schwed, et al.Journal of Medical Genetics|December 1, 1995
Further delineation of the partial proximal trisomy 10q syndromeC M Aalfs, J M Hoovers, M A Nieste-Otter, et al.Journal of Medical Genetics|December 1, 1995
The Irish cystic fibrosis databaseS M Cashman, A Patino, M G Delgado, et al.Journal of Medical Genetics|December 1, 1995
Familial café au lait spots: a variant of neurofibromatosis type 1D Abeliovich, Z Gelman-Kohan, S Silverstein, et al.Journal of Medical Genetics|December 1, 1995
Del(3) (p25.3) without phenotypic effectL A Knight, M H Yong, M Tan, et al.Journal of Medical Genetics|April 22, 2008
Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22K Pulli, K Karma, R Norio, et al.Pageof 649