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Human Genetics|June 19, 1979
Possible trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in 1qA SchinzelHuman Genetics|January 1, 1979
Dicentric Robertsonian translocation in man. 17 cases studied by R,C, and N bandingM G Mattei, J F Mattei, S Ayme, et al.Human Genetics|January 1, 1979
Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12)B Dallapiccola, L Chessa, P Vignetti, et al.Human Genetics|January 1, 1979
Sensitivity of Bloom's syndrome lymphocytes to ethyl methanesulfonateA B Krepinsky, J A Heddle, J GermanHuman Genetics|October 1, 1979
Ring chromosome 10 associated with multiple congenital malformationsG Simoni, F Rossella, L Dalprà, et al.Human Genetics|October 1, 1979
An r(22)(p11 leads to q13) in a moderately mentally retarded girlV Aller, J A Abrisqueta, M L de Torres, et al.Human Genetics|October 1, 1979
Reduced frequency of sister chromatid exchanges in human lymphocytes cultured with autologous serumP K Ghosh, R NandHuman Genetics|October 2, 1979
Cytogenetic effects of inactivated influenza virus on male germ cells of miceM A Thadani, H PolasaHuman Genetics|October 2, 1979
Polymorphism of alanine aminotransferase (E.C.2.7.6.1): common and rare allelesJ Kömpf, H RitterPageof 957