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American Journal of Medical Genetics|December 1, 1992
Acro-fronto-facio-nasal dysostosis: report of a new Brazilian familyA Richieri-Costa, M L Guion-Almeida, N A PagnanAmerican Journal of Medical Genetics|December 1, 1992
False-negative prenatal diagnosis of restrictive dermopathyB C Hamel, R Happle, P M Steylen, et al.American Journal of Medical Genetics|December 1, 1992
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasiaM Lerone, M Soliani, D Corea, et al.American Journal of Medical Genetics|December 1, 1992
Infantile autism--fragile X: molecular findings support genetic heterogeneityH Malmgren, K H Gustavson, J Wahlström, et al.American Journal of Medical Genetics|December 1, 1992
Limb anomalies following chorionic villus sampling: a registry based case-control studyP Mastroiacovo, L D Botto, D P Cavalcanti, et al.American Journal of Medical Genetics|April 1, 1992
Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastomaD Stambolian, B Sellinger, D Derrington, et al.American Journal of Medical Genetics|April 1, 1992
Vertebral hypersegmentation in a case of the VATER associationE A Wulfsberg, T L Phillips-Dawkins, R L ThomasAmerican Journal of Medical Genetics|April 1, 1992
High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from MoroccoA Rösler, E Leiberman, T CohenAmerican Journal of Medical Genetics|April 1, 1992
The second report of Knobloch syndromeA E Czeizel, P Göblyös, G Kustos, et al.American Journal of Medical Genetics|April 1, 1992
Autosomal dominant congenital laryngomalaciaM Shohat, Y Sivan, E Taub, et al.Pageof 854