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Absence of WNT4 gene mutation in a patient with MURCS association.
Shoar Z, Ganguly T, Anderson CE, De Luca F, Suarez E. Absence of WNT4 gene mutation in a patient with MURCS association. J Pediatr Endocrinol Metab. 2014 May; 27(5-6):555-9.
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subject areas
46, XX Disorders of Sex Development
Abnormalities, Multiple
Adolescent
Congenital Abnormalities
Female
Humans
Hyperandrogenism
Kidney Diseases
Mullerian Ducts
Obesity
Sex Chromosome Disorders
Syndrome
Ultrasonography
Uterus
Wnt4 Protein