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The Journal of Pediatrics|September 13, 2003
Thrombocytopenia in patients with chromosome 22q11.2 deletion syndromeScott Lawrence, Donna M McDonald-McGinn, Elaine Zackai, et al.Human Genetics|November 1, 1986
Complex chromosomal rearrangement and multiple spontaneous abortionsJ L Gorski, B S Emanuel, E H Zackai, et al.American Journal of Medical Genetics. Part A|October 5, 2020
Clinical variability of TUBB-associated disorders: Diagnosis through reanalysisDong Li, Kaitlyn M Shen, Elaine H Zackai, et al.American Journal of Medical Genetics. Part A|August 23, 2005
DiGeorge anomaly in a patient with isochromosome 18p born to a diabetic motherRalph J DeBerardinis, Livija Medne, Nancy B Spinner, et al.American Journal of Medical Genetics. Part A|May 23, 2012
1.9 Mb microdeletion of 21q22.11 within Braddock-Carey contiguous gene deletion syndrome region: dissecting the phenotypeKosuke Izumi, Susan S Brooks, Holly A Feret, et al.American Journal of Medical Genetics|May 22, 1995
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13N B Spinner, E Zackai, S D Cheng, et al.Journal of Medical Genetics|December 1, 1983
Osteoglophonic dwarfism in two generationsR I Kelley, P F Borns, D Nichols, et al.American Journal of Medical Genetics|February 5, 1998
Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalusJ S Du, L Bason, H Woffendin, et al.Clinical Genetics|November 1, 1979
Interstitial deletion 13q33 resulting from maternal insertional translocationB S Emanuel, E H Zackai, L Moreau, et al.Prenatal Diagnosis|January 1, 1984
Prenatal diagnosis of mosaicism 46,XX/46,XX,-21,+t(21q21q)W S Long, M T Mennuti, B S Emanuel, et al.Pageof 63