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The Journal of Pediatrics|August 1, 1975
The fetal trimethadione syndromeE H Zackai, W J Mellman, B Neiderer, 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.Journal of Medical Genetics|December 1, 1976
Abnormal chromosome 22 and recurrence of trisomy-22 syndromeB S Emanuel, E H Zackai, M M Aronson, et al.American Journal of Medical Genetics|January 1, 1979
Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23B S Emanuel, E H Zackai, D C Van Dyke, et al.American Journal of Medical Genetics|January 1, 1980
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunctionE H Zackai, B S EmanuelScience (New York, N.Y.)|May 14, 1971
Galactosemia: evidence for a structural gene mutationT A Tedesco, W J MellmanHuman Genetics|January 1, 1983
Characterization of normal and abnormal variants of galactose-1-phosphate uridylyltransferase (EC 2.7.7.12) by isoelectric focusingR I Kelley, H Harris, W J MellmanAmerican 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 ZackaiNeurofibromatosis|January 1, 1988
The Neurofibromatosis Clinic of the Children's Hospital of PhiladelphiaA C Obringer, E H Zackai, A T MeadowsPageof 23