(Q34413379)

2 August 2017

title

Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndrome (English)

1 reference

Xavier Estivill i Pallejà

2 August 2017

author

series ordinal

3

1 reference

2 August 2017

P Scambler

2

0 references

author name string

R Llevadot

series ordinal

1

1 reference

2 August 2017

M Pritchard

series ordinal

4

1 reference

2 August 2017

publication date

1 December 1996

1 reference

2 August 2017

number of pages

4

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

2 August 2017

volume

7

1 reference

2 August 2017

issue

12

1 reference

2 August 2017

page(s)

911-914

1 reference

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

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

A survey on intron and exon lengths

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

A human homolog of the S.cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

A catalogue of splice junction sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

Relationship between the total size of exons and introns in protein-coding genes of higher eukaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

Alternative splicing of calretinin mRNA leads to different forms of calretinin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

DiGeorge syndrome and 22q11 rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900268

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8995764

12 December 2020

inferred from PubMed ID database lookup

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8995764

12 December 2020

inferred from PubMed ID database lookup

Alternative splicing of endothelial cell fibronectin mRNA in the IIICS region. Functional significance.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8995764

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S003359900268

1 reference

2 August 2017

1 reference