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American Journal of Medical Genetics|July 15, 1994
Prenatal diagnosis in known fragile X carriersA Maddalena, B D Hicks, W C Spence, et al.
Human Genetics|July 1, 1991
Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridizationR Plattner, N A Heerema, S R Patil, et al.
The New England Journal of Medicine|September 8, 1983
Chromosomal translocation involving the immunoglobulin kappa-chain and heavy-chain loci in a child with chronic lymphocytic leukemiaJ A Sonnier, G R Buchanan, P N Howard-Peebles, et al.
Prenatal Diagnosis|March 1, 2000
Characterization and clinical implications of marker chromosomes identified at prenatal diagnosisM M Li, P N Howard-Peebles, L D Killos, et al.
Human Genetics|July 1, 1993
Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridizationR Plattner, N A Heerema, P N Howard-Peebles, et al.
Prenatal Diagnosis|October 1, 1987
Fetal karyotype following ascertainment of fetal anomalies by ultrasoundC G Palmer, J H Miles, P N Howard-Peebles, et al.
American Journal of Medical Genetics|November 24, 1999
Isolated bilateral anophthalmia in a girl with an apparently balanced de novo translocation: 46,XX,t(3;11)(q27;p11.2)R W Driggers, C J Macri, J Greenwald, et al.
American Journal of Medical Genetics|April 20, 1999
Age-related language characteristics of children and adolescents with fragile X syndromeG S Fisch, J J Holden, N J Carpenter, et al.
Human Genetics|September 1, 1988
The parental origin and mechanism of formation of three dicentric X chromosomesM C Phelan, L A Prouty, R E Stevenson, et al.
American Journal of Medical Genetics|August 9, 1996
Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: a prospective multicenter analysisG S Fisch, R Simensen, J Tarleton, et al.
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