PAX2 in 192 Chinese women with Müllerian duct abnormalities: Mutation analysis

Reproductive BioMedicine Online

Volumn 25, Issue 2, 2012, Pages 219-222

  Wang, Peng ^a,b,c   Zhao, Han ^a,b,c   Sun, Mei ^a,b,c   Li, Yuan ^d   Chen, Zi Jiang ^a,b,c  

^a SHANDONG PROVINCIAL HOSPITAL AFFILIATED TO SHANDONG UNIVERSITY   (China)

^b BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

^c Shandong Provincial Key Laboratory of Reproductive Medicine   (China)

^d CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

MRKH syndrome; M llerian duct abnormalities; mutation; paired box gene 2; polymerase chain reaction; single nucleotide polymorphism

Indexed keywords

TRANSCRIPTION FACTOR PAX2;

ADULT; ARTICLE; CHINESE; CONTROLLED STUDY; CORRELATION ANALYSIS; FEMALE; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; UTERINE AGENESIS; UTERUS BICORNIS; UTERUS DIDELPHYS; UTERUS MALFORMATION; UTERUS SEPTUS; UTERUS UNICORNIS;

BASE SEQUENCE; CHINA; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MOLECULAR SEQUENCE DATA; MULLERIAN DUCTS; PAX2 TRANSCRIPTION FACTOR; POINT MUTATION; PREGNANCY;

EID: 84864465964     PISSN: 14726483     EISSN: 14726491     Source Type: Journal    
DOI: 10.1016/j.rbmo.2012.04.010     Document Type: Article

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