(Q72660203)

English

Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences

scientific article published on 01 December 1993

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

ovotesticular disorder of sex development

1 reference

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author name string

U Kuhnle

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

H P Schwarz

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

U Löhrs

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

S Stengel-Ruthkowski

4

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Europe PubMed Central

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28 October 2019

H Cleve

5

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Europe PubMed Central

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28 October 2019

A Braun

6

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Europe PubMed Central

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28 October 2019

publication date

1 December 1993

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

92

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

6

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Europe PubMed Central

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28 October 2019

571-576

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

A possible common origin of "Y-negative" human XX males and XX true hermaphrodites

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gonads of human true hermaphrodites

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Y-chromosomal and autosomal testis-determining genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma testosterone in male puberty. II. hCG stimulation test in boys with hypospadia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

True hermaphroditism. A review of 41 cases with observations on testicular histology and function

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion map of the human Y chromosome based on DNA hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

17-hydroxyprogesterone, androstenedione, and testosterone in normal children and in prepubertal patients with congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic evidence equating SRY and the testis-determining factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic evidence that ZFY is not the testis-determining factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

True hermaphroditism in a 46,XY individual, caused by a postzygotic somatic point mutation in the male gonadal sex-determining locus (SRY): molecular genetics and histological findings in a sporadic case

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial true hermaphroditism in genetic females]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human XY female with a frame shift mutation in the candidate testis-determining gene SRY.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial XX chromosomal maleness does not arise from a Y chromosomal translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

True hermaphrodite siblings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial XX true hermaphroditism and the H-Y antigen

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex and the single Y

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA Binding Activity of Recombinant SRY from Normal Males and XY Females

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial true hermaphrodism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TRUE HERMAPHRODITES IN JAPAN. REPORT OF A CASE AND REVIEW OF THE LITERATURE

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male development of chromosomally female mice transgenic for Sry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8262517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00420941

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262517%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

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