(Q28261277)

2

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P Meinecke

3

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S Pedersen

4

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L Bolund

5

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C Brandt

6

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C Goodpasture

7

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P Guldberg

8

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K R Held

9

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H Reinwein

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

10

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language of work or name

English

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publication date

June 1993

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published in

Nature Genetics

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volume

4

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issue

2

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page(s)

170-4

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0693-170

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

Genetic evidence equating SRY and the testis-determining factor

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

Expression of a candidate sex-determining gene during mouse testis differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

Positional cloning: let's not call it reverse anymore

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

XY gonadal dysgenesis: Genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

A chromosome 17q de novo paracentric inversion in a patient with campomelic dysplasia; case report and etiologic hypothesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Campomelic dysplasia with sex reversal: morphological and cytogenetic studies of a case.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Sex-reversed XY females with campomelic dysplasia are H-Y negative

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Acampomelic campomelic dysplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Fine mapping of human 5S rRNA genes to chromosome 1q42.11→q42.13

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

A simple sequence repeat polymorphism at the human growth hormone locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Partial deletion of distal 17q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

XY sex-reversed campomelia - possibly an X-linked disorder?

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

On the parental origin of de novo mutation in man.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0693-170

1 reference

7 January 2021

High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Cytologic evidence for three human X-chromosomal segments escaping inactivation

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Assignment of the human gene for pregnancy-associated plasma protein A (PAPPA) to 9q33.1 by fluorescence in situ hybridization to mitotic and meiotic chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Preparation and bivariate analysis of suspensions of human chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Improved resolution of flow cytometric measurements of Hoechst- and chromomycin-A3-stained human chromosomes after addition of citrate and sulfite

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021

Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-170

7 January 2021