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J L Mandel

Showing results (141-150 of 257) with videos related to

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Ophthalmic Genetics|October 19, 2011
Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencingK Aliferis, S Hellé, G Gyapay, 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.
Cytogenetics and Cell Genetics|January 1, 1990
Report of the committee on the genetic constitution of the X chromosomeK E Davies, J L Mandel, A P Monaco, 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.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequencesJ L Mandel, B Arveiler, G Camerino, 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.
Nucleic Acids Research|February 11, 1989
A probe from an X-Y homology region detects RFLPs in Xq13-q22R P Feil, E Gillard, N A Affara, et al.
Pageof 26

Showing results (141-150 of 257) with videos related to

Sort By:
Pageof 26
Ophthalmic Genetics|October 19, 2011
Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencingK Aliferis, S Hellé, G Gyapay, 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.
Cytogenetics and Cell Genetics|January 1, 1990
Report of the committee on the genetic constitution of the X chromosomeK E Davies, J L Mandel, A P Monaco, 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.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequencesJ L Mandel, B Arveiler, G Camerino, 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.
Nucleic Acids Research|February 11, 1989
A probe from an X-Y homology region detects RFLPs in Xq13-q22R P Feil, E Gillard, N A Affara, et al.
Pageof 26