Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7 (Q67754465)

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17 September 2019

title

Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1740347%20AND%20SRC:MED&resulttype=core&format=json

X-linked congenital stationary night blindness

17 September 2019

main subject

0 references

1 reference

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13 November 2022

author name string

N. T. Bech-Hansen

1

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13 November 2022

B. J. Moore

2

1 reference

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13 November 2022

W. G. Pearce

3

1 reference

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13 November 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1740347

13 November 2022

publication date

1 February 1992

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full work available at URL

17 September 2019

https://api.elsevier.com/content/article/PII:0888754392903948?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

https://api.elsevier.com/content/article/PII:0888754392903948?httpAccept=text/plain

13 November 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

13 November 2022

1 reference

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17 September 2019

volume

12

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17 September 2019

issue

2

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17 September 2019

page(s)

409-411

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Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

17 September 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome

13 November 2022

2

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa

13 November 2022

4

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locus

13 November 2022

5

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

13 November 2022

6

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

13 November 2022

7

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Report of the committee on linkage and gene order

13 November 2022

8

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Report of the committee on the genetic constitution of the X chromosome

13 November 2022

12

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.

13 November 2022

14

1 reference

https://api.crossref.org/works/10.1016/0888-7543(92)90394-8

13 November 2022

Identifiers

1 reference

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17 September 2019

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