ACOG Committee Opinion No. 469: Carrier screening for fragile X syndrome.

Obstetrics and gynecology

Volumn 116, Issue 4, 2010, Pages 1008-1010

  American College of Obstetricians and Gynecologists Committee on Genetics, ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

FMR1 PROTEIN, HUMAN; FRAGILE X MENTAL RETARDATION PROTEIN;

ARTICLE; FEMALE; FRAGILE X SYNDROME; GENETICS; HETEROZYGOTE DETECTION; HUMAN; MUTATION; NUCLEOTIDE SEQUENCE;

DNA MUTATIONAL ANALYSIS; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; HETEROZYGOTE DETECTION; HUMANS; MUTATION;

EID: 77958157320     PISSN: None     EISSN: 1873233X     Source Type: Journal    
DOI: None     Document Type: Article

References (0)