(Q24312613)

English

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

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scholarly article

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

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Caenorhabditis elegans

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Ess-2 splicing factor homolog

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GOA release 2020-03-11

nervous system development

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GOA release 2020-03-11

Peter J Scambler

object named as

P Scambler

6

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author name string

P Rizzu

1

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E A Lindsay

2

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C Taylor

3

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H O'Donnell

4

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A Levy

5

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A Baldini

7

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language of work or name

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publication date

September 1996

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Mammalian Genome

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7

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9

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639-43

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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 22q11 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

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