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American Journal of Medical Genetics|September 1, 1983
Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisonsR C Juberg, P N MowreyAmerican Journal of Medical Genetics|March 1, 1984
Interstitial del(13q) associated with blindness and mental retardationR C Juberg, P N MowreyJournal of Medical Genetics|February 1, 1985
Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous abortersR C Juberg, J Knops, P N MowreyClinical Genetics|June 1, 1991
Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversionJ C Ramer, P N Mowrey, R L LaddaAmerican Journal of Medical Genetics|September 1, 1990
Neurologic manifestations in 18q- syndromeG Miller, P N Mowrey, K D Hopper, et al.American Journal of Medical Genetics|November 1, 1990
Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformationsJ C Ramer, P N Mowrey, D B Robins, et al.Journal of Medical Genetics|January 1, 1997
46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosisC P Venditti, N K Seese, G S Gerhard, et al.American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.Cancer Genetics and Cytogenetics|April 25, 2007
Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second caseC A Tirado, A M Meloni-Ehrig, T Edwards, et al.Pageof 1