(Q33678523)

English

Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193 (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

ORCID Public Data File 2021

author name string

R H Flomen

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

P A Gorman

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

R Vatcheva

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

J Groet

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

I Barisić

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

I Ligutić

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

D Sheer

7

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

D Nizetić

8

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 March 1997

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

191-195

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

A new bacteriophage P1-derived vector for the propagation of large human DNA fragments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Genetic heterogeneity in Rieger eye malformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Isolation and mapping of human chromosome 21 cDNA: progress in constructing a chromosome 21 expression map.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

A YAC contig map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Axenfeld-Rieger syndrome. A spectrum of developmental disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Evidence that Rieger syndrome maps to 4q25 or 4q27

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Rieger syndrome and interstitial 4q26 deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

The Rieger syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050891

21 June 2018

Pericentric inversion and partial monosomy 4q associated with congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion 4q and Rieger syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9132488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.34.3.191

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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