Familial transmission of the FMR1 CGG repeat

American Journal of Human Genetics

Volumn 59, Issue 6, 1996, Pages 1252-1261

  Nolin, Sarah L ^b   Lewis III, French A ^b   Ye, Ling Ling ^b   Houck Jr , George E ^b   Glicksman, Anne E ^b   Limprasert, Pornprot ^b   Li, Shu Yun ^b   Zhong, Nan ^b   Ashley, Allison E ^b   Feingold, Eleanor ^b   Sherman, Stephanie L ^b   Ted Brown, W ^a  

^a NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA; TRINUCLEOTIDE;

ALLELE; ARTICLE; FAMILIAL DISEASE; FEMALE; FRAGILE X SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MALE; MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ALLELES; ANALYSIS OF VARIANCE; CHROMOSOME FRAGILITY; FEMALE; FRAGILE X SYNDROME; HUMANS; MALE; PEDIGREE; POLYMERASE CHAIN REACTION; TRINUCLEOTIDE REPEATS;

EID: 19244362362     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Ashley AE, Sherman SL (1995) Population dynamics of a meiotic/mitotic expansion model for the fragile X syndrome. Am J Hum Genet 57:1414-1425
2. Ashley CT, Jrilkinson KD, Reines D, Warren ST (1993) FMR1 protein: conserved RNP family domains and selective binding. Science 262:563-565
3. Brown WT, Houck GE Jr, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, et al (1996a) Reverse mutations in the fragile X syndrome. Am J Med Genet 64:287-292
4. Brown WT, Houck GE Jr, Jeziorowska A, Levinson FN, Ding X, Dobkin C, Zhong N, et al (1993) Rapid fragile X carrier screening and prenatal diagnosis by a non-radioactive PCR test. JAMA 270:1569-1575
5. Brown WT, Jenkins EC (1992) The fragile X syndrome. In: Friedmann T (ed) Molecular genetic medicine, Academic Press, New York, pp 39-66