(Q52192462)

26 April 2018

title

Another critical region for deletion of 22q11: a study of 100 patients. (English)

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26 April 2018

author name string

Kurahashi H

1

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26 April 2018

Tsuda E

2

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26 April 2018

Kohama R

3

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26 April 2018

Nakayama T

4

1 reference

26 April 2018

Masuno M

5

1 reference

26 April 2018

Imaizumi K

6

1 reference

26 April 2018

Kamiya T

7

1 reference

26 April 2018

Sano T

8

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26 April 2018

Okada S

9

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26 April 2018

Nishisho I

10

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26 April 2018

publication date

1 October 1997

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26 April 2018

American Journal of Medical Genetics Part A

published in

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26 April 2018

volume

72

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26 April 2018

page(s)

180-185

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26 April 2018

issue

2

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26 April 2018

Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome

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

21 January 2018

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Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

21 January 2018

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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

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Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

21 January 2018

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Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region

21 January 2018

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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

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Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

21 January 2018

1 reference

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Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome

21 January 2018

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

21 January 2018

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Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

21 January 2018

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Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

21 January 2018

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DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin

21 January 2018

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Deletions within chromosome 22q11 in familial congenital heart disease

21 January 2018

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

21 January 2018

1 reference

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DiGeorge syndrome and 22q11 rearrangements

21 January 2018

1 reference

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High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes

21 January 2018

1 reference

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

21 January 2018

1 reference

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The immunocompetence of children with congenital heart disease

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(19971017)72:2<180::AID-AJMG10>3.0.CO;2-J

21 January 2018

Identifiers

DOI

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26 April 2018

PubMed ID

9382139

1 reference

26 April 2018