(Q67737752)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1733838%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

title

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1733838%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

1 reference

1

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17 September 2019

author name string

D L Thiselton

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1733838%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

J B Bateman

3

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17 September 2019

J T Ngo

4

1 reference

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17 September 2019

R S Sparkes

5

1 reference

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17 September 2019

M Coleman

6

1 reference

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17 September 2019

K E Davies

7

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17 September 2019

S S Bhattacharya

8

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17 September 2019

publication date

1 January 1992

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17 September 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1733838%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

volume

88

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17 September 2019

issue

3

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17 September 2019

page(s)

349-350

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https://scigraph.springernature.com/pub.10.1007/bf00197273

17 September 2019

exact match

0 references

cites work

Physical fine-mapping of a deletion spanning the Norrie gene

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

1 reference

12 December 2020

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

12 December 2020

Norrie disease resulting from a gene deletion: clinical features and DNA studies

1 reference

12 December 2020

Further linkage data on Norrie disease

1 reference

12 December 2020

Five polymorphic microsatellite VNTRs on the human X chromosome.

1 reference

12 December 2020

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

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the MAOA locus

1 reference

12 December 2020

Genetic and physical mapping around the properdin P gene

1 reference

12 December 2020

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

1 reference

12 December 2020

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

1 reference

12 December 2020

1 reference

12 December 2020

Recombinational event between Norrie disease and DXS7 loci

1 reference

12 December 2020

Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie disease

1 reference

12 December 2020

Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00197273

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1733838%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

17 September 2019

0 references

1 reference