Showing results (661-670 of 8,534) with videos related to
Sort By:
Pageof 854
American Journal of Medical Genetics|May 1, 1983
Discordance for the Kleeblattschädel anomaly in monozygotic twins with thanatophoric dysplasiaW A Horton, D J Harris, D L CollinsAmerican Journal of Medical Genetics|July 1, 1983
The Börjeson-Forssman-Lehmann syndromeL K Robinson, K L Jones, F Culler, et al.American Journal of Medical Genetics|July 3, 1995
L206W mutation of the cystic fibrosis gene, relatively frequent in French Canadians, is associated with atypical presentations of cystic fibrosisR Rozen, L Ferreira-Rajabi, L Robb, et al.American Journal of Medical Genetics|July 3, 1995
Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndromeK H Chrzanowska, W J Kleijer, M Krajewska-Walasek, et al.American Journal of Medical Genetics|January 2, 1995
Mediastinal teratoma and precocious puberty in a boy with mosaic Klinefelter syndromeA N Derenoncourt, M Castro-Magana, K L JonesAmerican Journal of Medical Genetics|January 16, 1995
Heterogeneity in Roberts syndromeD J Allingham-Hawkins, D J TomkinsAmerican Journal of Medical Genetics|October 1, 1994
Familial Dandy-Walker malformation associated with macrocephaly, facial anomalies, developmental delay, and brain stem dysgenesis: prenatal diagnosis and postnatal outcome in brothers. A new syndrome?D Chitayat, L Moore, M R Del Bigio, et al.American Journal of Medical Genetics|September 15, 1993
Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndromeR L Ladda, J Zonana, J C Ramer, et al.American Journal of Medical Genetics|July 17, 1995
Analysis of variability of clinical manifestations in Waardenburg syndromeJ E Reynolds, J M Meyer, B Landa, et al.American Journal of Medical Genetics|July 17, 1995
Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skullH M Saal, D I Bulas, J F Allen, et al.Pageof 854