(Q41759259)

8 October 2017

Physical fine-mapping of a deletion spanning the Norrie gene (English)

1 reference

8 October 2017

Xandra O. Breakefield

5

object named as

X O Breakefield

1 reference

8 October 2017

P J Diergaarde

1

1 reference

8 October 2017

B Wieringa

2

1 reference

8 October 2017

E M Bleeker-Wagemakers

3

1 reference

8 October 2017

K B Sims

4

1 reference

8 October 2017

H H Ropers

6

1 reference

8 October 2017

language of work or name

1 reference

1 December 1989

1 reference

8 October 2017

1 reference

8 October 2017

84

1 reference

8 October 2017

1

1 reference

8 October 2017

22-26

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00210665

8 October 2017

0 references

cites work

pG95 alpha 1-7dIII/RI, a single copy clone at Xp11.4 which recognises a TaqI polymorphism (DXS209).

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

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

1 reference

12 December 2020

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

1 reference

12 December 2020

An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146).

1 reference

12 December 2020

Further linkage data on Norrie disease

1 reference

12 December 2020

Norrie disease: Linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe

1 reference

12 December 2020

cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties

1 reference

12 December 2020

Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration

1 reference

12 December 2020

The use of a DNA marker for carrier diagnosis in an X-linked disorder: Norrie's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Regional localisation of X chromosome short arm probes

1 reference

12 December 2020

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

1 reference

12 December 2020

Separation of large DNA molecules by contour-clamped homogeneous electric fields

1 reference

12 December 2020

Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie disease

1 reference

12 December 2020

First demonstration of recombination between the gene for Norrie disease and probe L1.28.

1 reference

12 December 2020

Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism

1 reference

12 December 2020

Regional localization of 18 human X-linked DNA sequences

1 reference

12 December 2020

Structural Features of Human Monoamine Oxidase A Elucidated from cDNA and Peptide Sequences

1 reference

12 December 2020

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

1 reference

12 December 2020

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

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

Monoamine oxidase deficiency in males with an X chromosome deletion

1 reference

12 December 2020

Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes

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

Norrie disease gene is distinct from the monoamine oxidase genes.

1 reference

12 December 2020

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation

1 reference

12 December 2020

Audiological findings in Norrie's disease

1 reference

12 December 2020

1 reference

12 December 2020

A rapid method for the purification of DNA from blood

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/BF00210665

1 reference

Dimensions Publication ID

8 October 2017

0 references

1 reference