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M G Mattei

Showing results (191-200 of 427) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1994
S-laminin gene (Lams) maps to F1 band of mouse chromosome 9D Aberdam, M F Galliano, M G Mattei, 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.
Genomics|October 1, 1992
Localization of the genes for human inositol 1,4,5-trisphosphate 3-kinase A (ITPKA) and B (ITPKB) to chromosome regions 15q14-q21 and 1q41-q43, respectively, by in situ hybridizationC Erneux, N Roeckel, K Takazawa, et al.
Human Molecular Genetics|December 1, 1995
Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndromeA Levy, S Demczuk, A Aurias, et al.
Immunity|January 16, 1998
Genetic control of diabetes progressionA Gonzalez, J D Katz, M G Mattei, et al.
Genomics|September 1, 1991
Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region)N G Seidah, M G Mattei, L Gaspar, et al.
American Journal of Medical Genetics|February 1, 1991
Transmission of mental retardation with fragile X site by two normal transmitter brothersM C Pellissier, M A Voelckel, C Piquet, et al.
Blood|August 15, 1995
Molecular basis and expression of the LWa/LWb blood group polymorphismP Hermand, P Gane, M G Mattei, et al.
Human Genetics|August 31, 1977
A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter to p22::p22 to qter))J F Mattei, H Taramasco, M G Mattei, et al.
Pageof 43

Showing results (191-200 of 427) with videos related to

Sort By:
Pageof 43
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1994
S-laminin gene (Lams) maps to F1 band of mouse chromosome 9D Aberdam, M F Galliano, M G Mattei, 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.
Genomics|October 1, 1992
Localization of the genes for human inositol 1,4,5-trisphosphate 3-kinase A (ITPKA) and B (ITPKB) to chromosome regions 15q14-q21 and 1q41-q43, respectively, by in situ hybridizationC Erneux, N Roeckel, K Takazawa, et al.
Human Molecular Genetics|December 1, 1995
Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndromeA Levy, S Demczuk, A Aurias, et al.
Immunity|January 16, 1998
Genetic control of diabetes progressionA Gonzalez, J D Katz, M G Mattei, et al.
Genomics|September 1, 1991
Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region)N G Seidah, M G Mattei, L Gaspar, et al.
American Journal of Medical Genetics|February 1, 1991
Transmission of mental retardation with fragile X site by two normal transmitter brothersM C Pellissier, M A Voelckel, C Piquet, et al.
Blood|August 15, 1995
Molecular basis and expression of the LWa/LWb blood group polymorphismP Hermand, P Gane, M G Mattei, et al.
Human Genetics|August 31, 1977
A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter to p22::p22 to qter))J F Mattei, H Taramasco, M G Mattei, et al.
Pageof 43