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JOURNAL ARTICLE
RESEARCH SUPPORT, NON-U.S. GOV'T
Variants of the WNT7A gene in Chinese patients with müllerian duct abnormalities.
Fertility and Sterility 2012 Februrary
OBJECTIVE: To search for WNT7A gene mutations in a cohort of 191 Chinese Han patients with müllerian duct abnormalities (MDAs).
DESIGN: Phenotypic and mutational study.
SETTING: University hospital.
PATIENT(S): A total of 191 Chinese Han patients with MDAs and 192 healthy control individuals.
INTERVENTION(S): Genomic DNA extracted from blood samples, all coding regions amplified by polymerase chain reaction (PCR) then directly sequenced to screen variants.
MAIN OUTCOME MEASURE(S): Not applicable.
RESULT(S): The sequence analysis revealed one novel synonymous variant and three known single-nucleotide polymorphisms (SNPs).
CONCLUSION(S): The results indicate that mutations in the coding sequence of WNT7A are not responsible for müllerian duct abnormalities in the Chinese population.
DESIGN: Phenotypic and mutational study.
SETTING: University hospital.
PATIENT(S): A total of 191 Chinese Han patients with MDAs and 192 healthy control individuals.
INTERVENTION(S): Genomic DNA extracted from blood samples, all coding regions amplified by polymerase chain reaction (PCR) then directly sequenced to screen variants.
MAIN OUTCOME MEASURE(S): Not applicable.
RESULT(S): The sequence analysis revealed one novel synonymous variant and three known single-nucleotide polymorphisms (SNPs).
CONCLUSION(S): The results indicate that mutations in the coding sequence of WNT7A are not responsible for müllerian duct abnormalities in the Chinese population.
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