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Human Genetics|February 1, 1990
Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patientsK Fukuchi, K Tanaka, Y Kumahara, et al.Human Genetics|February 1, 1990
Analysis of the transgenome of MET transfectant cell lines reveals that MET activation is accompanied by an interstitial insertionP J Scambler, B Wainwright, M Ramsay, et al.Human Genetics|February 1, 1990
Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminizationU Müller, N R Schneider, J F Marks, et al.Human Genetics|February 1, 1990
Trisomy 18 mosaicism in an adult woman with normal intelligence and history of miscarriageE Gersdorf, B Utermann, G UtermannHuman Genetics|August 7, 2012
Causation and causal inference for genetic effectsStijn Vansteelandt, Christoph LangeHuman Genetics|August 14, 2012
Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyWuyan Chen, Zhi Xu, Miki Nishitani, et al.Human Genetics|May 10, 1979
Population genetic studies of the Aka pygmies (Central Africa): a survey of red cell and serum enzymesH Vergnes, A Sevin, J Sevin, et al.Human Genetics|May 23, 1979
An estimate of genetic risk from 8-methoxypsoralen photochemotherapyB A BridgesHuman Genetics|June 19, 1979
Paracentric inversion in the short arm of chromosome 1J Deroover, J P Fryns, J Haegeman, et al.Pageof 957