Mutations in SOX2 cause anophthalmia (Q34180637)

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Language	Label	Description	Also known as
English	Mutations in SOX2 cause anophthalmia	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mutations in SOX2 cause anophthalmia (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Caroline Hayward

7

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Europe PubMed Central

PubMed publication ID

31 July 2017

Veronica van Heyningen

10

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Europe PubMed Central

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31 July 2017

David FitzPatrick

object named as

David R FitzPatrick

11

0 references

author name string

Judy Fantes

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Nicola K Ragge

2

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Europe PubMed Central

PubMed publication ID

31 July 2017

Sally-Ann Lynch

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Niolette I McGill

4

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31 July 2017

J Richard O Collin

5

1 reference

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31 July 2017

Patricia N Howard-Peebles

6

1 reference

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PubMed publication ID

31 July 2017

Anthony J Vivian

8

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31 July 2017

Kathy Williamson

9

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31 July 2017

language of work or name

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publication date

3 March 2003

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31 July 2017

Nature Genetics

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31 July 2017

33

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31 July 2017

4

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31 July 2017

461-463

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31 July 2017

Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Bilateral microphthalmos with colobomatous orbital cyst and de-novo balanced translocation t(3;5)

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolated bilateral anophthalmia in a girl with an apparently balanced de novo translocation: 46,XX,t(3;11)(q27;p11.2).

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome arm painting probes

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

The cDNA sequence and chromosomal location of the human SOX2 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Embryonic expression of the chicken Sox2, Sox3 and Sox11 genes suggests an interactive role in neuronal development

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

The transcription factor cSox2 and Neuropeptide Y define a novel subgroup of amacrine cells in the retina

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Pairing SOX off: with partners in the regulation of embryonic development

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Multipotent cell lineages in early mouse development depend on SOX2 function

1 reference

https://api.crossref.org/works/10.1038%2FNG1120

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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