Showing results (121-130 of 170) with videos related to
Sort By:
Pageof 17
American Journal of Medical Genetics|January 1, 1980
Virilism as a late manifestation in the Bardet-Biedl syndromeR V Haning, I H Carlson, E F Gilbert, et al.American Journal of Medical Genetics|December 1, 1985
An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcaneiW R Osebold, D J Remondini, E L Lester, et al.European Journal of Pediatrics|October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 casesA L Kosseff, J Herrmann, E F Gilbert, et al.American Journal of Medical Genetics|April 14, 1997
Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian familyG Sorge, L Pavone, A Polizzi, et al.European Journal of Pediatrics|January 2, 1976
Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.American Journal of Medical Genetics|November 1, 1994
Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional casesB Angle, S Holgado, B K Burton, et al.European Journal of Pediatrics|August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.Pediatric Pathology|January 1, 1985
Familial hemophagocytic lymphohistiocytosis: report of four cases in two families and review of the literatureE F Gilbert, G M ZuRhein, S M Wester, et al.European Journal of Pediatrics|August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest diseaseL O Langer, M Gonzalez-Ramos, H Chen, et al.Pageof 17