Showing results (941-950 of 8,534) with videos related to
Sort By:
Pageof 854
American Journal of Medical Genetics|March 1, 1996
Epidemiological analysis of the association of congenital diaphragmatic hernia with upper-limb deficiencies: a primary polytopic developmental field defectM L Martínez-FríasAmerican Journal of Medical Genetics|March 1, 1996
Standard curves of chest circumference in achondroplasia and the relationship of chest circumference to respiratory problemsA G Hunter, C S Reid, R M Pauli, et al.American Journal of Medical Genetics|May 17, 1996
Follow-up of a familial translocation t(10;16) with an unusual segregation patternR G Resta, F Luthardt, R KapurAmerican Journal of Medical Genetics|May 17, 1996
Two patients with duplication of 17p11.2: the reciprocal of the Smith-Magenis syndrome deletion?A Brown, M C Phelan, S Patil, et al.American Journal of Medical Genetics|May 17, 1996
Novel findings in a patient with Weaver or a Weaver-like syndromeG Scarano, M Della Monica, F Lonardo, et al.American Journal of Medical Genetics|June 14, 1996
Proband and parent assistance in identifying relatives for cystic fibrosis carrier testingJ R Sorenson, B Cheuvront, A Bruning, et al.American Journal of Medical Genetics|June 14, 1996
A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritanceJ M Ceballos-Quintal, D Pinto-Escalante, I Castillo-ZapataAmerican Journal of Medical Genetics|June 14, 1996
Identical twin discordance for the Brachmann-de Lange syndrome revisitedG Carakushansky, M B Aguiar, M R Gonçalves, et al.American Journal of Medical Genetics|August 9, 1996
Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 geneJ Steyaert, M Borghgraef, E Legius, et al.American Journal of Medical Genetics|August 9, 1996
New findings in the behavioral profile of young FraX femalesM Borghgraef, S Umans, J Steyaert, et al.Pageof 854