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Journal of Medical Genetics|November 1, 1987
Fetal valproate syndrome: is there a recognisable phenotype?R M Winter, D Donnai, J Burn, et al.Journal of Medical Genetics|February 1, 1988
A combinatorial method for grouping cases with multiple malformationsR M Winter, R D Clark, K Ashley, et al.Journal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.Journal of Medical Genetics|December 1, 1989
Unknown syndrome: microcephaly, hypoplastic nose, exophthalmos, gum hyperplasia, cleft palate, low set ears, and osteosclerosisJ Raine, R M Winter, A Davey, et al.American Journal of Medical Genetics|October 1, 1993
Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2W Reardon, S P McManus, D Summers, et al.Clinical Genetics|September 1, 1980
Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further caseR M Winter, D M Swallow, M Baraitser, et al.Journal of Medical Genetics|January 1, 1991
Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'K D MacDermot, R M Winter, D Taylor, et al.American Journal of Medical Genetics|January 30, 1995
Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndromeW Reardon, R J Gibbons, R M Winter, et al.American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.Journal of Medical Genetics|November 1, 1991
Microtia and short stature: a new syndromeB Cohen, I K Temple, J C Symons, et al.Pageof 23