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Human Mutation|May 2, 2000
Mutations in the human TWIST geneGripp, Zackai, Stolle
Radiologic Clinics of North America|September 11, 2001
A pragmatic approach to the radiologic diagnosis of pediatric syndromes and skeletal dysplasiasR I Markowitz, E Zackai
Developmental Disabilities Research Reviews|July 19, 2008
Genetic counseling for the 22q11.2 deletionDonna M McDonald-McGinn, Elaine H Zackai
American Journal of Medical Genetics. Part A|September 4, 2010
Early onset mandibuloacral dysplasia due to compound heterozygous mutations in ZMPSTE24Zahid Ahmad, Elaine Zackai, Livija Medne, et al.
The Laryngoscope|June 1, 1994
Otologic manifestations of neurofibromatosisS Smullen, T Willcox, R Wetmore, et al.
American Journal of Medical Genetics. Part A|September 30, 2004
Ganglioglioma in a Sotos syndrome patient with an NSD1 deletionMatthew A Deardorff, Melissa Maisenbacher, Elaine H Zackai
American Journal of Medical Genetics|August 1, 1988
Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literatureM Münke, B S Emanuel, E H Zackai
Clinical Genetics|July 1, 1989
Holt-Oram syndrome associated with the hypoplastic left heart syndromeT A Glauser, E Zackai, P Weinberg, et al.
American Journal of Medical Genetics|July 1, 1987
Deletion of 2p: a cytogenetic and clinical updateJ Neidich, E Zackai, M Aronson, et al.
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