Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired (Q22003954)

GOA release 2020-03-11

1 reference

S A Brown

1

Stephen A.

Brown

1 reference

6 February 2023

D Warburton

2

Dorothy

Warburton

1 reference

6 February 2023

L Y Brown

3

Lucia Y.

Brown

1 reference

6 February 2023

C Y Yu

4

Chih-yu

Yu

1 reference

6 February 2023

E R Roeder

5

Elizabeth R.

Roeder

1 reference

6 February 2023

S Stengel-Rutkowski

6

Sabine

Stengel-Rutkowski

1 reference

6 February 2023

R C Hennekam

7

Raoul C.M.

Hennekam

1 reference

6 February 2023

M Muenke

8

Maximilian

Muenke

1 reference

Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.

6 February 2023

language of work or name

English

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publication date

October 1998

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published in

Nature Genetics

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volume

20

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issue

2

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page(s)

180-3

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cites work

1 reference

odd-paired: a zinc finger pair-rule protein required for the timely activation of engrailed and wingless in Drosophila embryos

21 January 2018

1 reference

Drosophila midgut morphogenesis requires the function of the segmentation gene odd-paired

21 January 2018

1 reference

The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation

21 January 2018

1 reference

Selection of cDNAs using chromosome-specific genomic clones: application to human chromosome 13

21 January 2018

1 reference

The mouse zic gene family. Homologues of the Drosophila pair-rule gene odd-paired.

21 January 2018

1 reference

Identification and characterization of Zic4, a new member of the mouse Zic gene family.

21 January 2018

1 reference

X-linked situs abnormalities result from mutations in ZIC3

21 January 2018

1 reference

Holoprosencephaly: a paradigm for the complex genetics of brain development.

21 January 2018

1 reference

Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly

21 January 2018

1 reference

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly

21 January 2018

1 reference

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

1 reference

Human developmental disorders and the Sonic hedgehog pathway

21 January 2018

1 reference

Gli/Zic factors pattern the neural plate by defining domains of cell differentiation.

21 January 2018

1 reference

Drosophila Krüppel protein is a transcriptional repressor.

21 January 2018

1 reference

Transcriptional repression by the Drosophila even-skipped protein: definition of a minimal repression domain

21 January 2018

1 reference

Murine Hox-1.11 homeobox gene structure and expression

21 January 2018

1 reference

MAZ, a zinc finger protein, binds to c-MYC and C2 gene sequences regulating transcriptional initiation and termination

21 January 2018

1 reference

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

21 January 2018

1 reference

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families

21 January 2018

1 reference

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

21 January 2018

1 reference

A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.

21 January 2018

1 reference

Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

21 January 2018

1 reference

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

21 January 2018

1 reference

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/2484

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