(Q60641499)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

congenital stationary night blindness

21 September 2019

main subject

0 references

X-linked congenital stationary night blindness

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

author name string

N T Bech-Hansen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

L L Field

2

1 reference

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21 September 2019

A M Schramm

3

1 reference

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21 September 2019

M Reedyk

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

N J Fraser

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

W G Pearce

7

1 reference

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21 September 2019

publication date

1 April 1990

1 reference

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21 September 2019

1 reference

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21 September 2019

volume

84

1 reference

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21 September 2019

issue

5

1 reference

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21 September 2019

page(s)

406-408

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00195809

21 September 2019

exact match

0 references

cites work

Report of the committee on the genetic constitution of the X and Y chromosomes

1 reference

12 December 2020

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

1 reference

12 December 2020

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

1 reference

12 December 2020

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis

1 reference

12 December 2020

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

12 December 2020

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

12 December 2020

Prenatal exclusion of Norrie disease with flanking DNA markers

1 reference

12 December 2020

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

1 reference

12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

12 December 2020

Syndrome of congenital high myopia with nyctalopia. Report of findings in 25 families

1 reference

12 December 2020

Congenital stationary night blindness with negative electroretinogram. A new classification

1 reference

12 December 2020

DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA

1 reference

12 December 2020

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

1 reference

12 December 2020

The photopic electroretinogram in congenital stationary night blindness with myopia

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00195809

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1969841%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference