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American Journal of Medical Genetics|April 14, 1997
Sibs with cleidocranial dysplasia born to normal parents: germ line mosaicism?E H Zackai, N H Robin, D M McDonald-McGinnNeurology|November 18, 1998
Polymicrogyria in chromosome 22 delection syndromeP M Bingham, D Lynch, D McDonald-McGinn, et al.American Journal of Human Genetics|May 1, 1978
Prenatal diagnosis of hypophosphatasia; genetic, biochemical, and clinical studiesR A Mulivor, M Mennuti, E H Zackai, et al.American Journal of Medical Genetics. Part A|February 18, 2017
10-year-old female with intragenic KANSL1 mutation, no KANSL1-related intellectual disability, and preserved verbal intelligenceColleen Keen, Carole Samango-Sprouse, Holly Dubbs, et al.Cancer Genetics and Cytogenetics|April 15, 1986
Childhood neurofibromatosis: risk factors for malignant diseaseM Schneider, A C Obringer, E Zackai, et al.American Journal of Medical Genetics|November 20, 2002
Correlation between abnormal cardiac physical examination and echocardiographic findings in neonates with Down syndromeDoff B McElhinney, Michele Straka, Elizabeth Goldmuntz, et al.Pediatrics|December 4, 2001
Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of ageD B McElhinney, D McDonald-McGinn, E H Zackai, et al.Pediatrics|November 1, 1975
Familial partial trisomy of the long arm of chromosome 10 (q24-26)H Moreno-Fuenmayor, E H Zackai, W J Mellman, et al.The Journal of Pediatrics|August 1, 1975
The fetal trimethadione syndromeE H Zackai, W J Mellman, B Neiderer, et al.American Journal of Medical Genetics|December 4, 1995
Analysis of clinical variation seen in patients with 18q terminal deletionsG Strathdee, E H Zackai, R Shapiro, et al.Pageof 63