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Human Genetics|December 1, 1996
Localization of the human phosphotyrosine phosphatase-related genes (h-PRL-1) to chromosome bands 1p35-p34, 17q12-q21, 11q24-q25 and 12q24M Montagna, O Serova, B S Sylla, et al.European Journal of Pediatrics|February 1, 1984
Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;p11)P Balestrazzi, M G Mattei, M A Baeteman, et al.Genomics|May 1, 1994
Molecular cloning, cDNA analysis, and localization of a monomer of the N-acetylglucosamine-specific receptor of the thyroid, NAGR1, to chromosome 19p13.3-13.2O Blanck, C Perrin, H Mziaut, et al.Nature|December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal maleG Camerino, M G Mattei, J F Mattei, et al.Human Genetics|January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8pJ F Mattei, M G Mattei, J P Ardissone, et al.Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|April 1, 1977
Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12J F Dor, J F Mattei, M G Mattei, et al.Genetical Research|June 1, 1989
Chromosomal localization of the mouse gene coding for vimentinM G Mattei, A Lilienbaum, L Z Lin, et al.The Biochemical Journal|May 15, 1995
Structural organization and chromosomal localization of the mouse collagenase type I geneM Schorpp, M G Mattei, I Herr, et al.Human Genetics|July 1, 1994
Chromosomal mapping of human adenylyl cyclase genes type III, type V and type VIN Haber, D Stengel, N Defer, et al.Archives Francaises De Pediatrie|February 1, 1975
[Trisomy 8 in mosaicism]F Giraud, J F Mattei, M Blanc-Pardigon, et al.Pageof 64