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Complete androgen insensitivity syndrome : Long-term medical, surgical, and psychosexual outcome

The journal of clinical endocrinology and metabolism, 2000-08, Vol.85 (8), p.2664-2669

2000

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ATTITUDES OF ADULT 46,XY INTERSEX PERSONS TO CLINICAL MANAGEMENT POLICIES

The Journal of urology, 2004-04, Vol.171 (4), p.1615-1619

2004

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Sequence of the Intron/Exon Junctions of the Coding Region of the Human Androgen Receptor Gene and Identification of a Point Mutation in a Family with Complete Androgen Insensitivity

Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (23), p.9534-9538

1989

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Ambiguous genitalia with perineoscrotal hypospadias in 46,XY individuals: long-term medical, surgical, and psychosexual outcome

Pediatrics (Evanston), 2002-09, Vol.110 (3), p.e31-e31

2002

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Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis

American journal of human genetics, 1992-11, Vol.51 (5), p.979-984

1992

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Deletion of the Steroid-Binding Domain of the Human Androgen Receptor Gene in One Family with Complete Androgen Insensitivity Syndrome: Evidence for Further Genetic Heterogeneity in this Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1988-11, Vol.85 (21), p.8151-8155

1988

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46,XY intersex individuals: phenotypic and etiologic classification, knowledge of condition, and satisfaction with knowledge in adulthood

Pediatrics (Evanston), 2002-09, Vol.110 (3), p.e32-e32

2002

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A Novel Mechanism for Coupling of m4 Muscarinic Acetylcholine Receptors to Calmodulin-Sensitive Adenylyl Cyclases: Crossover from G Protein-Coupled Inhibition to Stimulation

Biochemistry (Easton), 1994-02, Vol.33 (4), p.943-951

1994

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Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The New England journal of medicine, 1987-01, Vol.316 (4), p.178

1987

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The role of the sex-determining region Y gene in the etiology of 46,XX maleness

The journal of clinical endocrinology and metabolism, 1993-03, Vol.76 (3), p.690-695

1993

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Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity

Molecular endocrinology (Baltimore, Md.), 1990-12, Vol.4 (12), p.1759-1772

1990

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Assay of plasma testosterone during the first six months of life: importance of chromatographic purification of steroids

Clinical chemistry (Baltimore, Md.), 1995-08, Vol.41 (8 Pt 1), p.1146-1149

1995

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Evaluation of Boys with Marked Breast Development at Puberty

Clinical pediatrics, 1998-06, Vol.37 (6), p.367-371

1998

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McCune-Albright syndrome. Long-term follow-up

JAMA : the journal of the American Medical Association, 1986-12, Vol.256 (21), p.2980

1986

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Studies of the Locus for Androgen Receptor: Localization on the Human X Chromosome and Evidence for Homology with the Tfm Locus in the Mouse

Proceedings of the National Academy of Sciences - PNAS, 1981-10, Vol.78 (10), p.6339-6343

1981

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Congenital micropenis: long-term medical, surgical and psychosexual follow-up of individuals raised male or female

Hormone research, 2001-01, Vol.56 (1-2), p.3-11

2001

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Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesis

The journal of clinical endocrinology and metabolism, 1996-12, Vol.81 (12), p.4479-4483

1996

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Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis

The journal of clinical endocrinology and metabolism, 1993-05, Vol.76 (5), p.1248-1253

1993

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Regulation of cAMP-mediated gene transcription by wild type and mutated G-protein alpha subunits. Inhibition of adenylyl cyclase activity by muscarinic receptor-activated and constitutively activated G(o) alpha

The Journal of biological chemistry, 1994-11, Vol.269 (46), p.29146-29152

1994

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Comments about the need for prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1990-04, Vol.70 (4), p.836-837

MIGEON, C. J

1990

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The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1996-09, Vol.81 (9), p.3180-3190

1996

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Cloning and characterization of peter pan, a novel Drosophila gene required for larval growth

Molecular biology of the cell, 1999-06, Vol.10 (6), p.1733-1744

1999

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Congenital adrenal hyperplasia: long-term results following vaginal reconstruction

Fertility and sterility, 1986-12, Vol.46 (6), p.1011-1014

1986

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Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

The journal of clinical endocrinology and metabolism, 1986-05, Vol.62 (5), p.995-1002

1986

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Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Growth, development, and therapeutic considerations

Endocrinology and metabolism clinics of North America, 2001-03, Vol.30 (1), p.viii-206

2001

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Complete androgen insensitivity syndrome : Long-term medical, surgical, and psychosexual outcome

ATTITUDES OF ADULT 46,XY INTERSEX PERSONS TO CLINICAL MANAGEMENT POLICIES

Sequence of the Intron/Exon Junctions of the Coding Region of the Human Androgen Receptor Gene and Identification of a Point Mutation in a Family with Complete Androgen Insensitivity

Ambiguous genitalia with perineoscrotal hypospadias in 46,XY individuals: long-term medical, surgical, and psychosexual outcome

Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis

Deletion of the Steroid-Binding Domain of the Human Androgen Receptor Gene in One Family with Complete Androgen Insensitivity Syndrome: Evidence for Further Genetic Heterogeneity in this Syndrome

46,XY intersex individuals: phenotypic and etiologic classification, knowledge of condition, and satisfaction with knowledge in adulthood

A Novel Mechanism for Coupling of m4 Muscarinic Acetylcholine Receptors to Calmodulin-Sensitive Adenylyl Cyclases: Crossover from G Protein-Coupled Inhibition to Stimulation

Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The role of the sex-determining region Y gene in the etiology of 46,XX maleness

Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity

Assay of plasma testosterone during the first six months of life: importance of chromatographic purification of steroids

Evaluation of Boys with Marked Breast Development at Puberty

McCune-Albright syndrome. Long-term follow-up

Studies of the Locus for Androgen Receptor: Localization on the Human X Chromosome and Evidence for Homology with the Tfm Locus in the Mouse

Congenital micropenis: long-term medical, surgical and psychosexual follow-up of individuals raised male or female

Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesis

Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis

Regulation of cAMP-mediated gene transcription by wild type and mutated G-protein alpha subunits. Inhibition of adenylyl cyclase activity by muscarinic receptor-activated and constitutively activated G(o) alpha

Comments about the need for prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia

Cloning and characterization of peter pan, a novel Drosophila gene required for larval growth

Congenital adrenal hyperplasia: long-term results following vaginal reconstruction

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Growth, development, and therapeutic considerations

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