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M G Mattei

Showing results (231-240 of 427) with videos related to

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Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Development (Cambridge, England)|January 1, 1987
Mapping the mouse X chromosome: possible symmetry in the location of a family of sequences on the mouse X and Y chromosomesP Avner, C Bishop, L Amar, et al.
Genomics|January 1, 1993
Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridizationC Chevillard, B Attali, F Lesage, et al.
The EMBO Journal|November 1, 1990
Thyroid nuclear factor 1 (TTF-1) contains a homeodomain and displays a novel DNA binding specificityS Guazzi, M Price, M De Felice, et al.
Biochemistry|February 12, 1991
Gene structure and chromosomal localization of plasma kallikreinG Beaubien, I Rosinski-Chupin, M G Mattei, et al.
Genomics|April 1, 1994
Chromosomal localization of human RNA polymerase II subunit genesJ Acker, M G Mattei, M Wintzerith, et al.
Human Genetics|November 1, 1988
The gene encoding the large human neurofilament subunit (NF-H) maps to the q121-q131 region on human chromosome 22M G Mattei, A Dautigny, D Pham-Dinh, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome regionF Watrin, N Roëckel, L Lacroix, et al.
Pageof 43

Showing results (231-240 of 427) with videos related to

Sort By:
Pageof 43
Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Development (Cambridge, England)|January 1, 1987
Mapping the mouse X chromosome: possible symmetry in the location of a family of sequences on the mouse X and Y chromosomesP Avner, C Bishop, L Amar, et al.
Genomics|January 1, 1993
Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridizationC Chevillard, B Attali, F Lesage, et al.
The EMBO Journal|November 1, 1990
Thyroid nuclear factor 1 (TTF-1) contains a homeodomain and displays a novel DNA binding specificityS Guazzi, M Price, M De Felice, et al.
Biochemistry|February 12, 1991
Gene structure and chromosomal localization of plasma kallikreinG Beaubien, I Rosinski-Chupin, M G Mattei, et al.
Genomics|April 1, 1994
Chromosomal localization of human RNA polymerase II subunit genesJ Acker, M G Mattei, M Wintzerith, et al.
Human Genetics|November 1, 1988
The gene encoding the large human neurofilament subunit (NF-H) maps to the q121-q131 region on human chromosome 22M G Mattei, A Dautigny, D Pham-Dinh, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome regionF Watrin, N Roëckel, L Lacroix, et al.
Pageof 43