(Q28207829)

5

object named as

A de la Chapelle

0 references

author name string

E M Sankila

1

0 references

J A van den Hurk

3

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F P Cremers

4

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Sankila EM

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302003

10 September 2022

Tolvanen R

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302003

10 September 2022

van den Hurk JA

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302003

10 September 2022

Cremers FP

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302003

10 September 2022

de la Chapelle A

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302003

https://scigraph.springernature.com/pub.10.1038/ng0592-109

10 September 2022

language of work or name

English

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publication date

May 1992

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published in

Nature Genetics

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volume

1

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issue

2

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page(s)

109-13

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exact match

0 references

cites work

Cloning of a gene that is rearranged in patients with choroideraemia

1 reference

https://api.crossref.org/works/10.1038/NG0592-109

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0592-109

Choroideremia; clinical and genetic aspects

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

DXS26 (HU16) is located in Xq21.1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Haplotype and multipoint linkage analysis in Finnish choroideremia families

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Choroideremia: linkage analysis with physically mapped close DNA-markers

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-109

7 January 2021

Identifiers

DOI

10.1038/NG0592-109

1 reference

Consolidated OpenCitations Corpus – April 2017

5125658

5125658

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference