Czech family confirms the new 1p36.13‐1p36.12 microdeletion syndrome-Reference-Cited by-同舟云学术

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Czech family confirms the new 1p36.13‐1p36.12 microdeletion syndrome

Published:2022-06-21 Issue:3 Volume:102 Page:244-245
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Seeman Pavel¹²³,Čejnová Vlasta²,Černá Šárka²,Rennerová Ladislava⁴,Trková Marie³,Kofer Josef²,Laštůvková Jana²

Affiliation:

1. Department of Child Neurology 2nd Medical Faculty Charles University and University Hospital Motol Prague Prague Czech Republic

2. Department of Medical Genetics Masaryk Hospital Ústí nad Labem Usti nad Labem Czech Republic

3. Gennet s.r.o. Prague Czech Republic

4. Child Neurology Usti nad Labem Czech Republic

Funder

Ministerstvo Zdravotnictví Ceské Republiky

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14175

Reference1 articles.

1. A new 1p36.13‐1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis

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