(Q50847792)

23 March 2018

review article

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title

Abnormalities of gonadal differentiation. (English)

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23 March 2018

author name string

Berkovitz GD

series ordinal

1

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23 March 2018

Seeherunvong T

series ordinal

2

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23 March 2018

publication date

1 April 1998

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23 March 2018

Bailliere's clinical endocrinology and metabolism

published in

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23 March 2018

volume

12

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23 March 2018

issue

1

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23 March 2018

page(s)

133-142

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23 March 2018

Clinical and Pathologic Spectrum of 46,XY Gonadal Dysgenesis

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1 reference

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The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism

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7 January 2021

Abnormality of the X chromosome in human 46,XY female siblings with dysgenetic ovaries

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7 January 2021

A de novo mutation (Gln2Stop) at the 5' end of the SRY gene leads to sex reversal with partial ovarian function

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7 January 2021

Mutations inSRY andSOX9: Testis-determining genes

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7 January 2021

A cytogenetic investigation of inherited true hermaphroditism in BALB/cWt mice

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7 January 2021

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

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Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism

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7 January 2021

Disorders of sexual development

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7 January 2021

X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome

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7 January 2021

Pregnancy in a 46, XY patient

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7 January 2021

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

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7 January 2021

Two uses for old SOX.

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7 January 2021

True hermaphroditism with 46,XY karyotype and a point mutation in the SRY gene

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Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update

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Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype

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7 January 2021

The gonads of human true hermaphrodites

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Gonadoblastoma in infancy: Indications for early gonadectomy in 46XY gonadal dysgenesis

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7 January 2021

Dysgenesis of testicular and streak gonads in the syndrome of mixed gonadal dysgenesis: perspective derived from a clinicopathologic analysis of twenty-one cases

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7 January 2021

Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females.

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The anatomy and histology of XO human embryos and fetuses

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Familial 46,XX males coexisting with familial 46,XX true hermaphrodites in same pedigree

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XX true hermaphroditism in southern African blacks: exclusion of SRY sequences and uniparental disomy of the X chromosome

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7 January 2021

Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene

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7 January 2021

Molecular biologic analyses of tetragametic chimerism in a true hermaphrodite with 46,XX/46,XY

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7 January 2021

Abnormal sexual differentiation and neoplasia

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7 January 2021

Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite.

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7 January 2021

10.1016/S0950-351X(98)80512-0

Identifiers

DOI

1 reference

23 March 2018

1 reference

23 March 2018