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Cell|July 1, 1980
The ovalbumin gene family: structure of the X gene and evolution of duplicated split genesR Heilig, F Perrin, F Gannon, et al.Revue D'Epidemiologie Et De Sante Publique|January 1, 1995
[Comparative analysis of the costs of cytogenetic techniques and molecular biology techniques in the diagnosis of fragile X disease]I Hirtzlin, J L Mandel, J L Lanoé, et al.FEBS Letters|May 16, 1994
The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane proteinM Contreras, J Mosser, J L Mandel, et al.Human Molecular Genetics|November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsC Oudet, A Hanauer, P Clemens, et al.Genomics|August 1, 1991
Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresisR Fujita, A Hanauer, A Vincent, et al.American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyI Oberlé, D Drayna, G Camerino, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxiaR Fujita, A Hanauer, G Sirugo, et al.European Journal of Human Genetics : EJHG|May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasiaM C Vincent, V Biancalana, D Ginisty, et al.European Journal of Human Genetics : EJHG|January 15, 1999
Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)C Broccardo, N Troffer-Charlier, S Savary, et al.Pageof 20