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F Halal

Showing results (31-40 of 38) with videos related to

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American Journal of Medical Genetics|September 1, 1982
Metaphyseal dysplasia with maxillary hypoplasia and brachydactylyF Halal, J L Picard, D Raymond-Tremblay, et al.
American Journal of Medical Genetics|January 1, 1980
Acro-renal-mandibular syndromeF Halal, M F Desgranges, B Leduc, et al.
American Journal of Medical Genetics|August 1, 1992
Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: a new syndromeV M Der Kaloustian, N McIntosh, K Silver, et al.
Archives of Disease in Childhood|March 1, 1981
Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3C R Scriver, T Reade, F Halal, et al.
American Journal of Medical Genetics|June 1, 1992
Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20F Halal, D Chitayat, H Parikh, et al.
American Journal of Medical Genetics|January 1, 1993
Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?D Chitayat, S Haj-Chahine, H J Stalker, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Severe forms of Baraitser-Winter syndrome are caused by ACTB mutations rather than ACTG1 mutationsN Di Donato, A Rump, R Koenig, et al.
Pediatric Dermatology|February 1, 1988
Ruvalcaba-Myhre-Smith syndromeJ C Gretzula, O Hevia, L S Schachner, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
American Journal of Medical Genetics|September 1, 1982
Metaphyseal dysplasia with maxillary hypoplasia and brachydactylyF Halal, J L Picard, D Raymond-Tremblay, et al.
American Journal of Medical Genetics|January 1, 1980
Acro-renal-mandibular syndromeF Halal, M F Desgranges, B Leduc, et al.
American Journal of Medical Genetics|August 1, 1992
Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: a new syndromeV M Der Kaloustian, N McIntosh, K Silver, et al.
Archives of Disease in Childhood|March 1, 1981
Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3C R Scriver, T Reade, F Halal, et al.
American Journal of Medical Genetics|June 1, 1992
Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20F Halal, D Chitayat, H Parikh, et al.
American Journal of Medical Genetics|January 1, 1993
Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?D Chitayat, S Haj-Chahine, H J Stalker, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Severe forms of Baraitser-Winter syndrome are caused by ACTB mutations rather than ACTG1 mutationsN Di Donato, A Rump, R Koenig, et al.
Pediatric Dermatology|February 1, 1988
Ruvalcaba-Myhre-Smith syndromeJ C Gretzula, O Hevia, L S Schachner, et al.
Pageof 4