Showing results (441-450 of 9,587) with videos related to
Sort By:
Pageof 959
Human Genetics|March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutationsJ S Beck, A E Kwitek, P H Cogen, et al.Human Genetics|March 1, 1993
Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk populationC Stoll, B Dott, Y Alembik, et al.Human Genetics|March 1, 1993
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigreeA Sander, H Moser, S Liechti-Gallati, et al.Human Genetics|March 1, 1993
Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomasA Lindblom, L Skoog, T I Andersen, et al.Human Genetics|March 1, 1993
D21S210: a highly polymorphic (GT)n marker closely linked to the beta-amyloid protein precursor (APP) geneA C Warren, M G McInnis, M Kalaitsidaki, et al.Human Genetics|January 1, 1980
Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in FranceC Picat, J Etiemble, P Boivin, et al.Human Genetics|January 1, 1980
A new approach in the evaluation of chromosome variants in man. II. Pairs without Q or C (qh) variantsJ Azumi, Y Nakagome, S Oka, et al.Human Genetics|January 1, 1980
A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family membersA Smith, M NoelHuman Genetics|January 1, 1980
Chromosome studies on lymphocytes of patients under cytostatic therapy. II. Studies Using the BUDR-labelling technique in cytostatic interval therapyE Gebhart, B Windolph, F WopfnerHuman Genetics|January 1, 1980
Abnormal cerebral cortical convolutions in an XYY fetusG E Austin, R S SparkesPageof 959