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Journal of Medical Genetics|March 1, 1988
A reappraisal of the CHARGE associationC A Oley, M Baraitser, D B GrantAnnales De Genetique|January 1, 1994
Clinical identification of a human equivalent to the short ear (se) murine phenotypeD Lacombe, A Toutain, R J Gorlin, et al.Journal of Medical Genetics|January 1, 1996
FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13)J A Crolla, I Cross, N Atkey, et al.Genomics|January 1, 1993
Evidence for locus heterogeneity in autosomal dominant torsion dystoniaF Ahmad, M B Davis, H M Waddy, et al.Journal of Medical Genetics|March 1, 1997
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locusJ A Crolla, J E Cawdery, C A Oley, et al.Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.American Journal of Human Genetics|February 1, 1995
Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37L C Wilson, K Leverton, M E Oude Luttikhuis, et al.Human Genetics|June 1, 2000
Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseasesM Hargrave, K James, K Nield, et al.Pageof 1