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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.Journal of Substance Abuse Treatment|May 27, 2014
Legal factors associated with change in alcohol use and partner violence among offendersCory A Crane, Robert C Schlauch, Samuel W Hawes, 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.Genomics|July 1, 1988
Isolation and characterization of a family of sequences dispersed on the human X chromosomeB Bardoni, S Guioli, E Raimondi, et al.Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.Ophthalmic Genetics|October 19, 2011
Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencingK Aliferis, S Hellé, G Gyapay, et al.Pageof 32