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Aromatase excess syndromeas a model for genomic disorder: identification of molecular bases and phenotypic determinantsDOI 10.1186/1687-9856-2013-s1-o20
Clinical review 78: Aromatase deficiency in women and men: would you have predicted the phenotypes?Semantic proximity
Human gene mutations. Gene symbol: CYP19. Disease: Aromatase deficiency.Semantic proximity
A detailed molecular model for human aromataseSemantic proximity
Androgen receptor defects: historical, clinical, and molecular perspectives.Semantic proximity
Aromatase excess syndrome: a rare autosomal dominant disorder leading to pre- or peri-pubertal onset gynecomastia.Semantic proximity
A case of Aromatase deficiency due to a novel CYP19A1 mutationSemantic proximity
What are the indications for prenatal diagnosis in the androgen insensitivity syndrome? Facing clinical heterogeneity of phenotypes for the same genotype.Semantic proximity
Recognizing rare disorders: aromatase deficiency.Semantic proximity
Androgen resistance--the clinical and molecular spectrum.Semantic proximity
Aromatase excess syndrome: identification of cryptic duplications and deletions leading to gain of function of CYP19A1 and assessment of phenotypic determinants.Semantic proximity
The Aromatase Excess Syndrome Is Associated with Feminization of Both Sexes and Autosomal Dominant Transmission of Aberrant P450 Aromatase Gene TranscriptionSemantic proximity
Androgen insensitivity and the evolving genetic heterogeneity.Semantic proximity
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