(Q28198282)

2

0 references

Setsuko Noda

3

0 references

Shinsei Minoshima

4

0 references

Nobuyoshi Shimizu

Biochemical and Biophysical Research Communications

5

0 references

language of work or name

English

0 references

publication date

25 April 2003

0 references

published in

0 references

volume

304

0 references

issue

1

0 references

page(s)

184-90

0 references

cites work

DiGeorge syndrome: part of CATCH 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

A new concept of the cellular basis of immunity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Velo-cardio-facial syndrome: a review of 120 patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Prevalence of 22q11 microdeletion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

The DNA sequence of human chromosome 22

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Automated detection of point mutations using fluorescent sequence trace subtraction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Mouse myocilin (Myoc) gene expression in ocular tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

A conserved double-stranded RNA-binding domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Minor-groove recognition of double-stranded RNA by the double-stranded RNA-binding domain from the RNA-activated protein kinase PKR.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Characterization of a novel protein-binding module--the WW domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Towards prediction of cognate complexes between the WW domain and proline-rich ligands

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

NeW wrinkles for an old domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900554-0

10.1016/S0006-291X(03)00554-0

7 January 2021

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12705904

1 reference

Consolidated OpenCitations Corpus – April 2017