Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. (Q41149582)

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21 October 2019

title

Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region (English)

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21 October 2019

author name string

Datson NA

1

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21 October 2019

Semina E

2

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21 October 2019

van Staalduinen AA

3

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21 October 2019

Dauwerse HG

4

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21 October 2019

Meershoek EJ

5

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21 October 2019

Heus JJ

6

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21 October 2019

Frants RR

7

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21 October 2019

den Dunnen JT

8

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21 October 2019

Murray JC

9

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21 October 2019

van Ommen GJ

10

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21 October 2019

language of work or name

English

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publication date

1 December 1996

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American Journal of Human Genetics

21 October 2019

published in

1 reference

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21 October 2019

volume

59

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21 October 2019

issue

6

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21 October 2019

page(s)

1297-1305

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Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus

21 October 2019

cites work

1 reference

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High resolution restriction mapping of YACs using chromosome fragmentation

27 September 2017

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Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product.

27 September 2017

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

27 September 2017

1 reference

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Rieger syndrome revisited: experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-alpha functions resulting in dysmorphogenesis during embryonic mouse craniofacial morphogenesis

27 September 2017

1 reference

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A first-generation physical map of the human genome

27 September 2017

1 reference

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Genetic heterogeneity in Rieger eye malformation

27 September 2017

1 reference

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Position-effect variegation and the new biology of heterochromatin

27 September 2017

1 reference

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Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25)

27 September 2017

1 reference

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Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914859

A YAC contig map of the human genome

27 September 2017

1 reference

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The 1993-94 Généthon human genetic linkage map

27 September 2017

1 reference

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High-efficiency yeast artificial chromosome fragmentation vectors.

27 September 2017

1 reference

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Evidence that Rieger syndrome maps to 4q25 or 4q27

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914859

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914859

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

27 September 2017

1 reference

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Rieger syndrome and interstitial 4q26 deletion

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914859

Integrated human genome-wide maps constructed using the CEPH reference panel.

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914859

Interstitial deletion 4q and Rieger syndrome

19 August 2018

1 reference

12 December 2020

Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations

1 reference

12 December 2020

Methods for pulsed-field gel electrophoresis

1 reference

12 December 2020

Use of YAC fragmentation to delimit a duplicated region on human chromosome 21

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940275%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

PubMed publication ID

8940275

1 reference