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Showing results (391-400 of 520) with videos related to

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American Journal of Medical Genetics|August 22, 1997
Familial broad terminal phalanges with one individual showing additional anomaliesL Pavone, G Sorge, V Pavone, et al.
The New England Journal of Medicine|November 28, 1985
Perinatal mortality due to interaction of diphenhydramine and temazepamG A Kargas, S A Kargas, H J Bruyere, et al.
American Journal of Medical Genetics|March 13, 1995
Asplenia in two father-son pairsN M Lindor, W A Smithson, C A Ahumada, et al.
Fetal and Pediatric Pathology|June 7, 2006
"Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndromeL G Best, E Gilbert-Barness, D E Gerrard, et al.
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.
The Journal of Urology|June 19, 2007
Genitourinary anomalies of pediatric FG syndromeJames F Smith, Robert O Wayment, Patrick C Cartwright, 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.
Pageof 52

Showing results (391-400 of 520) with videos related to

Sort By:
Pageof 52
American Journal of Medical Genetics|August 22, 1997
Familial broad terminal phalanges with one individual showing additional anomaliesL Pavone, G Sorge, V Pavone, et al.
The New England Journal of Medicine|November 28, 1985
Perinatal mortality due to interaction of diphenhydramine and temazepamG A Kargas, S A Kargas, H J Bruyere, et al.
American Journal of Medical Genetics|March 13, 1995
Asplenia in two father-son pairsN M Lindor, W A Smithson, C A Ahumada, et al.
Fetal and Pediatric Pathology|June 7, 2006
"Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndromeL G Best, E Gilbert-Barness, D E Gerrard, et al.
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.
The Journal of Urology|June 19, 2007
Genitourinary anomalies of pediatric FG syndromeJames F Smith, Robert O Wayment, Patrick C Cartwright, 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.
Pageof 52