(Q67482186)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302031%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

title

Kallmann syndrome due to a translocation resulting in an X/Y fusion gene (English)

1 reference

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13 September 2019

1 reference

4

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13 September 2019

author name string

Guioli S

1

1 reference

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13 September 2019

Incerti B

2

1 reference

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13 September 2019

Zanaria E

3

1 reference

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13 September 2019

Franco B

5

1 reference

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13 September 2019

Taylor K

6

1 reference

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13 September 2019

Ballabio A

7

1 reference

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13 September 2019

Camerino G

8

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13 September 2019

publication date

1 August 1992

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13 September 2019

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13 September 2019

volume

1

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13 September 2019

page(s)

337-340

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13 September 2019

issue

5

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https://scigraph.springernature.com/pub.10.1038/ng0892-337

13 September 2019

exact match

0 references

cites work

X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Long-range restriction map of the terminal part of the short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Human-mouse cell hybrid with human multiple Y chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Long-range physical mapping around the human steroid sulfatase locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Physical mapping of genes and sequences at the end of the human X chromosome short arm.

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Selective cloning and sequence analysis of the human L1 (LINE-1) sequences which transposed in the relatively recent past

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Localization of the X inactivation centre on the human X chromosome in Xq13.

1 reference

https://api.crossref.org/works/10.1038%2FNG0892-337

7 January 2021

Identifiers

DOI

10.1038/NG0892-337

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302031%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference