(Q37854599)

24 August 2017

title

Retinal dystrophy in the oculo-auricular syndrome due to HMX1 mutation (English)

1 reference

24 August 2017

author

François-Xavier Borruat

series ordinal

3

object named as

F-X Borruat

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24 August 2017

V Vaclavik

1

1 reference

24 August 2017

D F Schorderet

series ordinal

2

1 reference

24 August 2017

F L Munier

series ordinal

4

1 reference

24 August 2017

publication date

18 March 2011

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24 August 2017

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24 August 2017

volume

32

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24 August 2017

issue

2

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24 August 2017

page(s)

114-117

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Cloning, characterization, and mapping of the mouse homeobox gene Hmx1

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2011.562955

Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2011.562955

ISCEV Standard for full-field clinical electroretinography (2008 update).

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2011.562955

The Marshall M. Parks memorial lecture: making sense of early-onset childhood retinal dystrophies--the clinical phenotype of Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2011.562955

10.3109/13816810.2011.562955

21 January 2018

Identifiers

DOI

1 reference

24 August 2017

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