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The EMBO Journal|December 20, 1988
The chicken dystrophin cDNA: striking conservation of the C-terminal coding and 3' untranslated regions between man and chickenC Lemaire, R Heilig, J L MandelHuman Molecular Genetics|November 11, 1999
A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) proteinB Bardoni, A Schenck, J L MandelJournal of Medical Genetics|May 1, 1994
Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onsetY Trottier, V Biancalana, J L MandelHuman Genetics|February 1, 1990
An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin geneC Oudet, R Heilig, J L MandelNucleic Acids Research|December 20, 1979
DNA methylation: correlation with DNase I sensitivity of chicken ovalbumin and conalbumin chromatinM T Kuo, J L Mandel, P ChambonAmerican Journal of Medical Genetics|February 17, 2001
FMR1 gene and fragile X syndromeB Bardoni, J L Mandel, G S FischNucleic Acids Research|March 11, 1983
Repetitive satellite-like sequences are present within or upstream from 3 avian protein-coding genesL Maroteaux, R Heilig, D Dupret, et al.Genomics|February 1, 1990
A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genesR Feil, P Aubourg, R Heilig, et al.Nature 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.Pageof 20