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Science (New York, N.Y.)|August 12, 1988
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia lociL M Davis, R Stallard, G H Thomas, et al.Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.Genomics|March 15, 1996
Physical mapping of 49 microsatellite markers on chromosome 19 and correlation with the genetic linkage mapI Reguigne-Arnould, S Faure, M Chery, et al.American Journal of Human Genetics|April 1, 1989
A deletion map of the WAGR region on chromosome 11M Gessler, G H Thomas, P Couillin, et al.Cytogenetics and Cell Genetics|January 1, 1994
The gene encoding myeloid alpha-3-fucosyl-transferase (FUT4) is located between D1 1S388 and D11S919 on 11q21I Reguigne, M R James, C W Richard, et al.Genomics|October 1, 1992
Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patientsB Plougastel, P Couillin, V Blanquet, et al.Cytogenetics and Cell Genetics|January 1, 1995
Relative positions of two clusters of human alpha-L-fucosyltransferases in 19q (FUT1-FUT2) and 19p (FUT6-FUT3-FUT5) within the microsatellite genetic map of chromosome 19I Reguigne-Arnould, P Couillin, R Mollicone, et al.Annales De Genetique|January 1, 1987
From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalitiesM Plachot, J de Grouchy, A M Junca, et al.Annales De Genetique|January 1, 1992
Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridizationP Couillin, J Zucman, E Le Guern, et al.Human Genetics|August 1, 1986
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determinationE Mornet, J Boue, M Raux-Demay, et al.Pageof 7