CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds (Q28272409)

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English	CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds	scientific article

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scholarly article

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CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds (English)

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object named as

Ohad S Birk

6

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author name string

Udy Bar-Yosef

1

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Izzeldin Abuelaish

2

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Tamar Harel

3

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Neta Hendler

4

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Rivka Ofir

5

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language of work or name

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publication date

September 2004

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115

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4

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302-9

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A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

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inferred from PubMed ID database lookup

Isolated "clinical anophthalmia" in an extensively affected Arab kindred

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

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Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vertebrate eye development as modeled in Drosophila

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

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Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32.

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential interactions of eyeless and twin of eyeless with the sine oculis enhancer.

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of Chx10 and Chx10-1 in the developing chicken retina

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in SOX2 cause anophthalmia

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pax genes and eye organogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic rescue of cell number in a mouse model of microphthalmia: interactions between Chx10 and G1-phase cell cycle regulators

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian homologues of the Drosophila eye specification genes

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https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

1 reference

https://pubmed.ncbi.nlm.nih.gov/15257456

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-004-1154-2

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