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Obstetrics and Gynecology

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

Carrier screening for fragile X syndrome

[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

FOLLITROPIN; FRAGILE X MENTAL RETARDATION PROTEIN;

AMNIOCENTESIS; AUTISM; DEVELOPMENTAL DISORDER; DNA DETERMINATION; DNA TRANSCRIPTION; FAMILY HISTORY; FOLLITROPIN BLOOD LEVEL; FRAGILE X SYNDROME; GENE MUTATION; GENETIC COUNSELING; GENETIC SCREENING; HUMAN; INHERITANCE; MENTAL DEFICIENCY; NOTE; POLYMERASE CHAIN REACTION; PREMATURE OVARIAN FAILURE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SOUTHERN BLOTTING; ADULT; ALLELE; ARTICLE; FEMALE; GENETIC ASSOCIATION; MAJOR CLINICAL STUDY; NERVE DEGENERATION; UNITED STATES;

EID: 77957220436 PISSN: 00297844 EISSN: None Source Type: Journal
DOI: 10.1097/AOG.0b013e3181fae884 Document Type: Note

Times cited : (40)

References (11)

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2
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3
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9
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