Evidence that methylation of the FMR-1 locus is responsible for variable phenotypic expression of the fragile X syndrome

American Journal of Human Genetics

Volumn 53, Issue 4, 1993, Pages 800-809

  McConkie Rosell, A ^a   Lachiewicz, A M ^a   Spiridigliozzi, G A ^a   Tarleton, J ^a   Schoenwald, S ^a   Phelan, M C ^a   Goonewardena, P ^a   Ding, X ^a   Brown, W T ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME FRAGILITY; CHROMOSOME MOSAICISM; CLINICAL ARTICLE; COGNITIVE DEFECT; DNA METHYLATION; FRAGILE X SYNDROME; GENE LOCUS; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; PHENOTYPE; PRIORITY JOURNAL; PSYCHOLOGIC TEST;

ADULT; CHROMOSOME MAPPING; DNA; FEMALE; FRAGILE X SYNDROME; HUMAN; MALE; METHYLATION; MIDDLE AGE; NERVE TISSUE PROTEINS; PEDIGREE; PHENOTYPE; PSYCHOLOGICAL TESTS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; VARIATION (GENETICS);

EID: 0027486670     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)