FMR1 and the fragile X syndrome: human genome epidemiology review.

Crawford DC, Acuña JM, Sherman SL
Genet Med. 2001 3 (5): 359-71

PMID: 11545690 · PMCID: PMC4493892 · DOI:10.1097/00125817-200109000-00006

MeSH Terms (14)

European Continental Ancestry Group Female Fragile X Mental Retardation Protein Fragile X Syndrome Gene Frequency Genetic Testing Genome, Human Heterozygote Humans Male Mutation Nerve Tissue Proteins RNA-Binding Proteins Trinucleotide Repeats

Connections (1)

This publication is referenced by other Labnodes entities:

Links