A Lunkes|J L Mandel - JoVE Visualize

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Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984

Genetic mapping of the human X chromosome by using restriction fragment length polymorphismsD Drayna, K Davies, D Hartley, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.

American Journal of Human Genetics|February 1, 1988

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesB Arveiler, I Oberlé, A Vincent, et al.

The EMBO Journal|July 1, 1985

Extensive DNA sequence homologies between the human Y and the long arm of the X chromosomeD Geldwerth, C Bishop, G Guellaën, et al.

Biochimie|January 1, 1993

Adrenoleukodystrophy gene: unexpected homology to a protein involved in peroxisome biogenesisP Aubourg, J Mosser, A M Douar, et al.

American Journal of Human Genetics|March 1, 1992

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypesG Sirugo, B Keats, R Fujita, et al.

American Journal of Medical Genetics|April 1, 1992

Direct DNA analysis of fragile X syndrome in Spanish pedigreesI Tejada, E Mornet, V Biancalana, et al.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994

X-linked adrenoleukodystrophy gene: identification of a candidate gene by positional cloningA M Douar, J Mosser, C O Sarde, et al.

Human Molecular Genetics|November 1, 1993

Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophyN Cartier, C O Sarde, A M Douar, et al.

Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|September 1, 1989

[The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA]A Roth, D Klein, F Paccolat, et al.

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Showing results (101-110 of 198) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984

Genetic mapping of the human X chromosome by using restriction fragment length polymorphismsD Drayna, K Davies, D Hartley, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.

American Journal of Human Genetics|February 1, 1988

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesB Arveiler, I Oberlé, A Vincent, et al.

The EMBO Journal|July 1, 1985

Extensive DNA sequence homologies between the human Y and the long arm of the X chromosomeD Geldwerth, C Bishop, G Guellaën, et al.

Biochimie|January 1, 1993

Adrenoleukodystrophy gene: unexpected homology to a protein involved in peroxisome biogenesisP Aubourg, J Mosser, A M Douar, et al.

American Journal of Human Genetics|March 1, 1992

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypesG Sirugo, B Keats, R Fujita, et al.

American Journal of Medical Genetics|April 1, 1992

Direct DNA analysis of fragile X syndrome in Spanish pedigreesI Tejada, E Mornet, V Biancalana, et al.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994

X-linked adrenoleukodystrophy gene: identification of a candidate gene by positional cloningA M Douar, J Mosser, C O Sarde, et al.

Human Molecular Genetics|November 1, 1993

Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophyN Cartier, C O Sarde, A M Douar, et al.

Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|September 1, 1989

[The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA]A Roth, D Klein, F Paccolat, et al.

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