Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome. [electronic resource]
Producer: 20170503Description: 590-6 p. digitalISSN:- 1399-0004
- 46, XX Disorders of Sex Development -- genetics
- Base Sequence
- Codon, Nonsense
- Congenital Abnormalities -- genetics
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genetic Predisposition to Disease -- genetics
- Genotype
- Humans
- Mullerian Ducts -- abnormalities
- Mutation
- Mutation, Missense
- Retrospective Studies
- Syndrome
- Wnt Proteins -- genetics
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Publication Type: Journal Article
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