Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles

Human Genetics

Volumn 107, Issue 2, 2000, Pages 195-196

  Castellví Bel, Sergi ^a   Fernández Burriel, Miguel ^b   Rifé, Maria ^a   Jiménez, Dolores ^a   Mallolas, Judith ^a   Sánchez, Aurora ^a   Ramos, Feliciano ^c   Milà, Montserrat ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b HOSPITAL UNIVERSITARIO MATERNO INFANTIL DE CANARIAS   (Spain)

^c UNIVERSITY OF ZARAGOZA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN;

ALLELE; ARTICLE; CHROMOSOME MOSAICISM; CONTROLLED STUDY; FMR1 GENE; FRAGILE X SYNDROME; GENE; GENE MUTATION; GENETIC SCREENING; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

EID: 0033817364     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390000349     Document Type: Article

References (6)

1. Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: Identification of a case of FRAXE-associated mental retardation
2. The intermediate alleles of the fragile X CGG repeat in patients with mental retardation
3. An n-allele model for progressive amplification in the FMR1 locus
4. Population screening at the FRAXA and FRAXE loci: Molecular analyses of boys with learning difficulties and their mothers
5. The fragile X syndrome
6. Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique