Showing results (81-90 of 309) with videos related to
Sort By:
Pageof 31
Human Genetics|April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosomeA Vincent, C Kretz, I Oberlé, et al.Human Genetics|June 1, 1988
Chromosome localization and polymorphism of an oestrogen-inducible gene specifically expressed in some breast cancersJ P Moisan, M G Mattei, J L MandelJournal Fur Entwicklungspolitik : JEP|January 1, 1995
The uprooting of people, migration, and labor force experiences: Ecuador 1982 and 1990L A Brown, J L Mandel, V A LawsonAmerican Journal of Human Genetics|August 1, 1991
Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombinationC Oudet, R Heilig, A Hanauer, et al.Biochimica Et Biophysica Acta|June 20, 1990
Avian kidney mitochondrial hemeprotein P-4501 alpha: isolation, characterization and NADPH-ferredoxin reductase-dependent activityM L Mandel, S J Swartz, J G GhazarianNature Genetics|May 1, 1993
Origin of the expansion mutation in myotonic dystrophyG Imbert, C Kretz, K Johnson, et al.Nucleic Acids Research|May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long armM Koenig, G Camerino, R Heilig, et al.Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.Nucleic Acids Research|July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y geneR Heilig, R Muraskowsky, C Kloepfer, et al.Journal of Medical Genetics|December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutationF Rousseau, D Heitz, I Oberlé, et al.Pageof 31