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J F Mattei

Showing results (141-150 of 202) with videos related to

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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.
Pediatrie|January 1, 1992
[Vitamin D-resistant rickets type II: apropos of 2 cases]G Simonin, B Chabrol, E Moulene, 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.
Human Genetics|October 1, 1988
Assignment of the human hap retinoic acid receptor RAR beta gene to the p24 band of chromosome 3M G Mattei, H de Thé, J F Mattei, et al.
Archives Francaises De Pediatrie|December 1, 1977
[Clouston's ectodermal dysplasia. A case report with biochemical study of keratin]F Giraud, J F Mattei, M Rolland, et al.
Acta Paediatrica Scandinavica|July 1, 1982
Erythrocyte superoxide dismutase and redox enzymes in trisomy 21J F Mattei, M A Baeteman, A Baret, et al.
Annales D'Endocrinologie|January 1, 1977
[Apparent internal male pseudo-hermaphroditism. Gynecomastia. Negative gonad surgical research. Caryotype 46, XX. Presence of H-Y antigen (author's transl)]J Vague, J Guidon, J F Mattei, et al.
Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.
Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.
Human Genetics|December 1, 1986
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14-q21M G Mattei, Y Colin, C Le Van Kim, et al.
Pageof 21

Showing results (141-150 of 202) with videos related to

Sort By:
Pageof 21
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.
Pediatrie|January 1, 1992
[Vitamin D-resistant rickets type II: apropos of 2 cases]G Simonin, B Chabrol, E Moulene, 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.
Human Genetics|October 1, 1988
Assignment of the human hap retinoic acid receptor RAR beta gene to the p24 band of chromosome 3M G Mattei, H de Thé, J F Mattei, et al.
Archives Francaises De Pediatrie|December 1, 1977
[Clouston's ectodermal dysplasia. A case report with biochemical study of keratin]F Giraud, J F Mattei, M Rolland, et al.
Acta Paediatrica Scandinavica|July 1, 1982
Erythrocyte superoxide dismutase and redox enzymes in trisomy 21J F Mattei, M A Baeteman, A Baret, et al.
Annales D'Endocrinologie|January 1, 1977
[Apparent internal male pseudo-hermaphroditism. Gynecomastia. Negative gonad surgical research. Caryotype 46, XX. Presence of H-Y antigen (author's transl)]J Vague, J Guidon, J F Mattei, et al.
Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.
Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.
Human Genetics|December 1, 1986
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14-q21M G Mattei, Y Colin, C Le Van Kim, et al.
Pageof 21