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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.Journal of Medical Genetics|November 1, 1992
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.Revue Neurologique|December 19, 2000
[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.Human Molecular Genetics|June 1, 1994
The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kbF Duclos, F Rodius, K Wrogemann, et al.Annals of Botany|October 26, 2005
Genecology of Douglas fir in western Oregon and WashingtonJ Bradley St Clair, Nancy L Mandel, Kenneth W Vance-BorlandProceedings of the National Academy of Sciences of the United States of America|July 5, 2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PA Schenck, B Bardoni, A Moro, et al.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.Pageof 31