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M Chery

Showing results (21-30 of 26) with videos related to

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American Journal of Medical Genetics|August 15, 1994
Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivationN Abbadi, C Philippe, M Chery, et al.
Journal of Clinical Microbiology|October 1, 1984
Bacteriuria screening by direct bioluminescence assay of ATPR B Schifman, M Wieden, J Brooker, et al.
American Journal of Human Genetics|July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionZ Chettouh, M F Croquette, B Delobel, et al.
American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.
Human Mutation|August 3, 2000
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in FranceM Claustres, C Guittard, D Bozon, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
American Journal of Medical Genetics|August 15, 1994
Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivationN Abbadi, C Philippe, M Chery, et al.
Journal of Clinical Microbiology|October 1, 1984
Bacteriuria screening by direct bioluminescence assay of ATPR B Schifman, M Wieden, J Brooker, et al.
American Journal of Human Genetics|July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionZ Chettouh, M F Croquette, B Delobel, et al.
American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.
Human Mutation|August 3, 2000
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in FranceM Claustres, C Guittard, D Bozon, et al.
Pageof 3