FMR1 in global populations

American Journal of Human Genetics

Volumn 58, Issue 3, 1996, Pages 513-522

  Kunst, Catherine B ^a   Zerylnick, Chris ^a   Karickhoff, Laurie ^a   Eichler, Evan ^b   Bullard, Jennifer ^a   Chalifoux, Maryse ^c   Holden, Jeanette J A ^c   Torroni, Antonio ^d   Nelson, David L ^b   Warren, Stephen T ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c QUEEN S UNIVERSITY   (Canada)

^d SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CODON; DNA SEQUENCE; FRAGILE X SYNDROME; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; PRIORITY JOURNAL; X CHROMOSOME DOMINANT DISORDER;

ALLELES; BASE SEQUENCE; CONTINENTAL POPULATION GROUPS; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; GENE FREQUENCY; HAPLOTYPES; HUMANS; MALE; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; PHYLOGENY; POLYMORPHISM, GENETIC; RNA-BINDING PROTEINS; SEQUENCE ANALYSIS, DNA; TRINUCLEOTIDE REPEATS;

EID: 19144367229     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Arinami T, Asano M, Kobayashi K, Yanagi H, Hamaguchi H (1993) Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate. Hum Genet 92:431-436
2. Ashley CT, Warren ST (1995) Trinucleotide repeat expansion and human disease. Annu Rev Genet 29:703-728
3. Ashley CT, Wilkinson KD, Reines D, Warren ST (1993) FMR1 protein: conserved RNP family domains and selective RNA binding. Science 262:563-566
4. Ballinger SW, Schurr TG, Torroni A, Can YY, Hodge JA, Hassan K, Chen KH, et al (1992) Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations. Genetics 130:139-152
5. Brown WT, Houck GE, Jeziorowska A, Levinson FN, Ding X, Dobkin C, Zhong N, et al (1993) Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test. JAMA 13:1569-157527
6. Burke JR, Ikeuchi T, Koide R, Tsuji S, Yamada M, Pericak-Vance MA, Vance JM (1994) Dentatorubral-pallidoluysian atrophy and Haw River syndrome. Lancet 344:1711-1712