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Annales De Genetique|January 1, 1984
De novo del(3)(q2800)M C Alvarez Arratia, H Rivera, M Möller, et al.Annales De Genetique|January 1, 1981
Regional localization of the genes for human HEXB. PGK, GALA. HPRT, G6PD by somatic cell hybridizationD Weil, V C Nguyen, R Rebourcet, et al.Annales De Genetique|January 1, 1984
The structural gene for transferrin (TF) maps to 3q21----3qterC Huerre, G Uzan, K H Grzeschik, et al.Annales De Genetique|January 1, 1984
Deficiency 10p. Report of a case and exclusion mapping of the hexokinase 1 locus to band 10p11.2C Danesino, F Lo Curto, G Bonfant, et al.Annales De Genetique|January 1, 1984
Tetrasomy 18p: a distinctive syndromeH Rivera, M Möller, A Hernández, et al.Annales De Genetique|January 1, 1984
Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin)C Turleau, J de Grouchy, F Chavin-Colin, et al.Annales De Genetique|January 1, 1984
Trisomy 3p syndrome. Report of a new case, due to a chromosomal insertionE Orye, G LaureysAnnales De Genetique|January 1, 1984
Simplified chromosome preparations from chorionic villi obtained by choriocentesis or derived from induced abortionsD Pitmon, P Extermann, P Graff, et al.Annales De Genetique|January 1, 1980
[46,XX,r(18), + mar karyotype in the niece of a leukemic patient with trisomy 21 and cri du chat chromosome (author's transl)]L Koulischer, Y Gillerot, J RichardAnnales De Genetique|January 1, 1983
Sister chromatid exchange distribution in various human tissues exposed to MMC and BrdUA McNally, M RayPageof 129