Showing results (11-20 of 299) with videos related to
Sort By:
Pageof 30
American Journal of Medical Genetics|July 15, 1994
Towards identification of X-linked mental retardation genes: a proposalJ L MandelJournal of Medical Genetics|November 10, 2000
Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?U Salat, B Bardoni, D Wöhrle, et al.Human Molecular Genetics|August 13, 1998
A cellular model that recapitulates major pathogenic steps of Huntington's diseaseA Lunkes, J L MandelGrowth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|May 12, 2004
Fragile X mental retardation syndrome: from pathogenesis to diagnostic issuesJ L Mandel, V BiancalanaNucleic Acids Research|December 20, 1979
DNA methylation: organ specific variations in the methylation pattern within and around ovalbumin and other chicken genesJ L Mandel, P ChambonThe EMBO Journal|November 1, 1984
The glyceraldehyde 3 phosphate dehydrogenase gene family: structure of a human cDNA and of an X chromosome linked pseudogene; amazing complexity of the gene family in mouseA Hanauer, J L MandelCurrent Opinion in Neurobiology|February 7, 1998
Deciphering the cause of Friedreich ataxiaM Koenig, J L MandelNature Reviews. Genetics|September 5, 2001
Monogenic causes of X-linked mental retardationJ Chelly, J L MandelCurrent Opinion in Genetics & Development|June 1, 1992
Molecular genetics of the fragile-X syndrome: a novel type of unstable mutationJ L Mandel, D HeitzThe Veterinary Clinics of North America. Small Animal Practice|July 10, 2007
Calcium homeostasis in thyroid disease in dogs and catsPatricia A SchenckPageof 30