Submicroscopic deletions at 13q32.1 cause congenital microcoria (Q35266333)

25772937

7 August 2017

title

Submicroscopic deletions at 13q32.1 cause congenital microcoria (English)

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7 August 2017

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language of work or name

English

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publication date

12 March 2015

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25772937

American Journal of Human Genetics

7 August 2017

published in

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page(s)

631-639

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Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome

6 June 2020

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