Molecular analysis of the androgen receptor gene in 52 patients with complete or partial androgen insensitivity syndrome: a collaborative study.

Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome.

Point mutations detected in the androgen receptor gene of three men with partial androgen insensitivity syndrome.

Complete androgen insensitivity syndrome.

A novel mutation of androgen receptor gene in complete androgen insensitivity syndrome.

Different types of androgen receptor mutations in patients with complete androgen insensitivity syndrome.

An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity.

Genetic analysis of a family with complete androgen insensitivity syndrome.

Partial Androgen Insensitivity Syndrome Presenting with Gynecomastia.

A unique point mutation in the androgen receptor gene in a family with complete androgen insensitivity syndrome.

DNA linkage analysis and studies of the androgen receptor gene in a large kindred with complete androgen insensitivity.

Partial androgen insensitivity: the Reifenstein syndrome revisited.

Complete androgen insensitivity syndrome in three sisters.

A missense mutation in the androgen receptor gene causing androgen insensitivity syndrome in a Chinese family.

Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene.

Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity.

Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome.

Prenatal prediction of androgen insensitivity syndrome using exon 1 polymorphism of the androgen receptor gene.

Polycystic ovary syndrome woman with heterozygous androgen receptor gene mutation who gave birth to a child with androgen insensitivity syndrome.

A frame-shift mutation in the androgen receptor gene causes complete androgen insensitivity in the testicular-feminized mouse.

Partial androgen insensitivity syndrome: a diagnostic and therapeutic dilemma.

Point mutation in the steroid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndrome (CAIS).

Complete Androgen Insensitivity Syndrome in Three Generations of Indian Pedigree.

A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian family.

A novel insA2933 causes premature termination of translation and is accompanied by overexpression of truncated androgen receptor gene in a patient with complete androgen insensitivity syndrome.

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Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome.

Point mutations detected in the androgen receptor gene of three men with partial androgen insensitivity syndrome.

Complete androgen insensitivity syndrome.

A novel mutation of androgen receptor gene in complete androgen insensitivity syndrome.

Different types of androgen receptor mutations in patients with complete androgen insensitivity syndrome.

An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity.

Genetic analysis of a family with complete androgen insensitivity syndrome.

Partial Androgen Insensitivity Syndrome Presenting with Gynecomastia.

A unique point mutation in the androgen receptor gene in a family with complete androgen insensitivity syndrome.

DNA linkage analysis and studies of the androgen receptor gene in a large kindred with complete androgen insensitivity.

Partial androgen insensitivity: the Reifenstein syndrome revisited.

Complete androgen insensitivity syndrome in three sisters.

A missense mutation in the androgen receptor gene causing androgen insensitivity syndrome in a Chinese family.

Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene.

Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity.

Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome.

Prenatal prediction of androgen insensitivity syndrome using exon 1 polymorphism of the androgen receptor gene.

Polycystic ovary syndrome woman with heterozygous androgen receptor gene mutation who gave birth to a child with androgen insensitivity syndrome.

A frame-shift mutation in the androgen receptor gene causes complete androgen insensitivity in the testicular-feminized mouse.

Partial androgen insensitivity syndrome: a diagnostic and therapeutic dilemma.

Point mutation in the steroid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndrome (CAIS).

Complete Androgen Insensitivity Syndrome in Three Generations of Indian Pedigree.

A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian family.

A novel insA2933 causes premature termination of translation and is accompanied by overexpression of truncated androgen receptor gene in a patient with complete androgen insensitivity syndrome.

Molecular analysis of the androgen receptor gene in 52 patients with complete or partial androgen insensitivity syndrome: a collaborative study.

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