(Q48056033)

8 February 2018

title

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region. (English)

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8 February 2018

author name string

Galili N

1

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8 February 2018

Baldwin HS

2

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8 February 2018

Lund J

3

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8 February 2018

Reeves R

4

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8 February 2018

Gong W

5

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8 February 2018

Wang Z

6

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8 February 2018

Roe BA

7

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8 February 2018

Emanuel BS

8

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8 February 2018

Nayak S

9

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8 February 2018

Mickanin C

10

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8 February 2018

Budarf ML

11

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8 February 2018

Buck CA

12

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8 February 2018

publication date

1 January 1997

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8 February 2018

published in

Genome Research

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8 February 2018

volume

7

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8 February 2018

issue

1

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8 February 2018

page(s)

17-26

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8 February 2018

Characterization of a novel murine testis-specific serine/threonine kinase

cites work

1 reference

Gastrulation in the mouse: the role of the homeobox gene goosecoid

21 January 2018

1 reference

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

21 January 2018

1 reference

The spectrum of the DiGeorge syndrome

21 January 2018

1 reference

A sequence assembly and editing program for efficient management of large projects

21 January 2018

1 reference

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

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes

21 January 2018

1 reference

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

21 January 2018

1 reference

General method for amplifying regions of very high G+C content

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2

21 January 2018

1 reference

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

Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region

21 January 2018

1 reference

Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11.

21 January 2018

1 reference

Neural crest and normal development: a new perspective

21 January 2018

1 reference

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

21 January 2018

1 reference

The mouse severe combined immune deficiency (scid) mutation is closely linked to the B-cell-specific developmental genes VpreB and lambda 5.

21 January 2018

1 reference

Comparative map for mice and humans

21 January 2018

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Chromosome engineering in mice

21 January 2018

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Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome

21 January 2018

1 reference

Striking sequence similarity over almost 100 kilobases of human and mouse T–cell receptor DNA

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1101/GR.7.1.17

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8 February 2018

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8 February 2018