The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia. (Q34091503)

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11 November 2019

title

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia (English)

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11 November 2019

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9

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11 November 2019

author name string

Braybrook C

1

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11 November 2019

Doudney K

2

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11 November 2019

Marçano AC

3

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11 November 2019

Arnason A

4

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11 November 2019

Bjornsson A

5

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11 November 2019

Patton MA

6

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11 November 2019

Goodfellow PJ

7

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11 November 2019

Moore GE

8

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language of work or name

English

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publication date

1 October 2001

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11 November 2019

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11 November 2019

volume

29

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11 November 2019

issue

2

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11 November 2019

page(s)

179-183

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https://scigraph.springernature.com/pub.10.1038/ng730

11 November 2019

exact match

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cites work

The geographical distribution of neural tube defects and oral clefts

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7 January 2021

Genetics of craniofacial development and malformation

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7 January 2021

Sex-linked inheritance of cleft palate

1 reference

7 January 2021

Mendelian inheritance of isolated nonsyndromic cleft palate

1 reference

7 January 2021

X-linked cleft palate

1 reference

7 January 2021

A further X-linked isolated nonsyndromic cleft palate family with a nonexpressing obligate affected male

1 reference

7 January 2021

Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds

1 reference

7 January 2021

Linkage of an X-chromosome cleft palate gene

1 reference

7 January 2021

The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X

1 reference

7 January 2021

Molecular characterization of a new human T-box gene (TBX22) located in xq21.1 encoding a protein containing a truncated T-domain

1 reference

7 January 2021

The T-box gene family

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7 January 2021

Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.

1 reference

7 January 2021

Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region

1 reference

7 January 2021

Molecular cloning and characterization of a highly conserved human 67-kDa laminin receptor pseudogene mapping to Xq21.3.

1 reference

7 January 2021

Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.

1 reference

7 January 2021

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

1 reference

7 January 2021

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

1 reference

7 January 2021

Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela

1 reference

7 January 2021

Expression pattern of the mouse T gene and its role in mesoderm formation

1 reference

7 January 2021

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

1 reference

7 January 2021

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

T-targets: clues to understanding the functions of T-box proteins

1 reference

7 January 2021

Transforming growth factor-beta 3 is required for secondary palate fusion

1 reference

7 January 2021

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG730

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11559848%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

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