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American Journal of Medical Genetics|August 1, 1994
Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndromeJ A Delach, S S Rosengren, L Kaplan, et al.Cytogenetics and Cell Genetics|January 1, 1979
Assignment of a gene for uridine diphosphate galactose-4-epimerase to human chromosome 1 by somatic cell hybridization, with evidence for a regional assignment to 1pter yields 1p21P A Benn, T B Shows, G G D'Ancona, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 9, 2003
Cost analysis of Down syndrome screening in advanced maternal ageJ Hartnett, A F Borgida, P A Benn, et al.American Journal of Human Genetics|March 1, 1997
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3V Greger, J H Knoll, J Wagstaff, et al.Somatic Cell Genetics|November 1, 1981
Reversion from deficiency of galactose-1-phosphate uridylytransferase (GALT) in an SV40-transformed human fibroblast lineP A Benn, R I Kelley, W J Mellman, et al.Biochemical and Biophysical Research Communications|May 28, 1993
Altered epidermal growth factor signal transduction in activated Ha-ras-transformed human keratinocytesL L Chen, R Narayanan, M S Hibbs, et al.Prenatal Diagnosis|July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studiesL Y Hsu, S Kaffe, E C Jenkins, et al.Prenatal Diagnosis|March 1, 1997
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlationsL Y Hsu, M T Yu, R L Neu, et al.Pageof 6