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The New England Journal of Medicine|December 12, 1985

Isolation of HTLV-III from cerebrospinal fluid and neural tissues of patients with neurologic syndromes related to the acquired immunodeficiency syndromeD D Ho, T R Rota, R T Schooley, et al.

Antimicrobial Agents and Chemotherapy|July 1, 1993

pol mutations conferring zidovudine and didanosine resistance with different effects in vitro yield multiply resistant human immunodeficiency virus type 1 isolates in vivoJ J Eron, Y K Chow, A M Caliendo, et al.

FEBS Letters|February 26, 1996

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.

Human Molecular Genetics|December 1, 1996

A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982

Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.

Neuromuscular Disorders : NMD|May 5, 1998

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.

Brain : a Journal of Neurology|October 8, 1998

Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain)M Urtasun, A Sáenz, C Roudaut, et al.

American Journal of Human Genetics|June 19, 1998

Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43P Berthon, A Valeri, A Cohen-Akenine, et al.

Neurology|May 1, 1997

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.

Journal of Medical Genetics|June 1, 1997

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.

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Showing results (171-180 of 185) with videos related to

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Pageof 19

The New England Journal of Medicine|December 12, 1985

Isolation of HTLV-III from cerebrospinal fluid and neural tissues of patients with neurologic syndromes related to the acquired immunodeficiency syndromeD D Ho, T R Rota, R T Schooley, et al.

Antimicrobial Agents and Chemotherapy|July 1, 1993

pol mutations conferring zidovudine and didanosine resistance with different effects in vitro yield multiply resistant human immunodeficiency virus type 1 isolates in vivoJ J Eron, Y K Chow, A M Caliendo, et al.

FEBS Letters|February 26, 1996

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.

Human Molecular Genetics|December 1, 1996

A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982

Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.

Neuromuscular Disorders : NMD|May 5, 1998

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.

Brain : a Journal of Neurology|October 8, 1998

Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain)M Urtasun, A Sáenz, C Roudaut, et al.

American Journal of Human Genetics|June 19, 1998

Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43P Berthon, A Valeri, A Cohen-Akenine, et al.

Neurology|May 1, 1997

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.

Journal of Medical Genetics|June 1, 1997

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.

Pageof 19