(Q42687641)

English

Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB).

scientific article published on January 1995

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB). (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

congenital disorder

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congenital stationary night blindness

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author name string

W Berger

1

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

G van Duijnhoven

2

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

A Pinckers

3

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

A Smits

4

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

H H Ropers

5

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

F Cremers

6

1 reference

Europe PubMed Central

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4 November 2017

publication date

1 January 1995

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Europe PubMed Central

PubMed publication ID

4 November 2017

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

95

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Europe PubMed Central

PubMed publication ID

4 November 2017

1

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Europe PubMed Central

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4 November 2017

67-70

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Europe PubMed Central

PubMed publication ID

4 November 2017

X-linked congenital stationary night blindness. Review and report of a family with hyperopia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the candidate gene for Norrie disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosomal recessive night blindness and tilted disk anomaly. A case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital stationary night blindness with negative electroretinogram. A new classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable expressivity in X-linked congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis in X-linked congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00225077

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

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