(Q68328468)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1684563%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type (English)

1 reference

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23 September 2019

1 reference

A A Bergen

1

1 reference

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23 September 2019

C Samanns

2

1 reference

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23 September 2019

E J Schuurman

3

1 reference

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23 September 2019

L van Osch

4

1 reference

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23 September 2019

D B van Dorp

5

1 reference

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23 September 2019

A J Pinckers

6

1 reference

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23 September 2019

E Bakker

7

1 reference

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23 September 2019

A Gal

8

1 reference

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23 September 2019

G J van Ommen

9

1 reference

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23 September 2019

E M Bleeker-Wagemakers

10

1 reference

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23 September 2019

publication date

1 December 1991

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23 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1684563%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

volume

88

1 reference

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23 September 2019

issue

2

1 reference

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23 September 2019

page(s)

162-166

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00206065

23 September 2019

exact match

0 references

cites work

Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresis

1 reference

12 December 2020

BclI RFLP at the DXS16 locus

1 reference

12 December 2020

An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry

1 reference

12 December 2020

Choroideremia-locus maps between DXS3 and DXS11 on Xq

1 reference

12 December 2020

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

1 reference

12 December 2020

Long-range restriction map of the terminal part of the short arm of the human X chromosome

1 reference

12 December 2020

X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene

1 reference

12 December 2020

Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.

1 reference

12 December 2020

Report of the committee on linkage and gene order

1 reference

12 December 2020

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

1 reference

12 December 2020

Identical twins discordant for Kallmann's syndrome

1 reference

12 December 2020

XmnI polymorphism of the human STS gene.

1 reference

12 December 2020

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

1 reference

12 December 2020

Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

1 reference

12 December 2020

Long-range physical mapping around the human steroid sulfatase locus

1 reference

12 December 2020

Ocular albinism and Xg

1 reference

12 December 2020

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

12 December 2020

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).

1 reference

12 December 2020

A long range restriction map of the distal human X chromosome short arm around the steroid sulfatase locus

1 reference

12 December 2020

An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome

1 reference

12 December 2020

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis

1 reference

12 December 2020

A decisive electrophysiological test for human albinism

1 reference

12 December 2020

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

12 December 2020

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

12 December 2020

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00206065

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1684563%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference