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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
authors with profiles
Francesco De Luca
Absence of WNT4 gene mutation in a patient with MURCS association.