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American Journal of Medical Genetics|November 15, 1993
Brachmann-de Lange syndrome with normal IQH M Saal, C A Samango-Sprouse, L A Rodnan, et al.American Journal of Medical Genetics|July 17, 1995
Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skullH M Saal, D I Bulas, J F Allen, et al.Journal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 1, 1995
Neonatal intensive care as a locus for ethical decisionsH M SaalThe Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 1, 1992
Clinician activism and ethical restraints in providing treatment: preventive as opposed to reconstructive approachesH M SaalAmerican Journal of Medical Genetics|August 1, 1992
New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sistersS G Kaler, A M Garrity, H J Stern, et al.American Journal of Medical Genetics|December 18, 1995
Neurodevelopmental profile of infants and toddlers with oculo-auriculo-vertebral spectrum and the correlation of prognosis with physical findingsM S Cohen, C A Samango-Sprouse, H J Stern, et al.Clinical Dysmorphology|July 1, 1995
Ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosumH M Saal, D I BulasAmerican Journal of Medical Genetics|March 3, 1997
Acampomelic campomelic dysplasia: further radiographic variationsR B Glass, K N RosenbaumClinical Genetics|June 1, 1991
A chromosome 17q de novo paracentric inversion in a patient with campomelic dysplasia; case report and etiologic hypothesisR Maraia, H M Saal, D WangsaPageof 7