Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans (Q24312613)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans	scientific article

Statements

scholarly article

0 references

Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans (English)

0 references

Caenorhabditis elegans

0 references

Ess-2 splicing factor homolog

1 reference

GOA release 2020-03-11

nervous system development

1 reference

GOA release 2020-03-11

Peter J Scambler

object named as

P Scambler

6

0 references

author name string

P Rizzu

1

0 references

E A Lindsay

2

0 references

C Taylor

3

0 references

H O'Donnell

4

0 references

A Levy

5

0 references

A Baldini

7

0 references

language of work or name

0 references

publication date

September 1996

0 references

Mammalian Genome

0 references

7

0 references

9

0 references

639-43

0 references

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

The scanning model for translation: an update

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Chromosome engineering in mice

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

The C. elegans genome sequencing project: a beginning

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

An expression-independent catalog of genes from human chromosome 22.

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

Mapping of the Tuple1 Gene to Mouse Chromosome 16A-B1

1 reference

https://api.crossref.org/works/10.1007%2FS003359900197

21 January 2018

DiGeorge syndrome and 22q11 rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and molecular study of DiGeorge sequence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BEAUTY: an enhanced BLAST-based search tool that integrates multiple biological information resources into sequence similarity search results

1 reference

https://pubmed.ncbi.nlm.nih.gov/8703114

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24312613&oldid=2175225474"