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7p21.3 together with a 12p13.32 deletion in a patient with microcephaly—does 12p13.32 locus possibly comprises a candidate gene region for microcephaly?

Affiliation
Croatian Institute for Brain Research, School of Medicine, University of Zagreb
Rincic, Martina;
Affiliation
Croatian Institute for Brain Research, School of Medicine, University of Zagreb
Rados, Milan;
Affiliation
Croatian Institute for Brain Research, School of Medicine, University of Zagreb
Kopic, Janja;
Affiliation
Croatian Institute for Brain Research, School of Medicine, University of Zagreb
Krsnik, Zeljka;
GND
115661239
ORCID
0000-0003-1672-3054
Affiliation
Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics
Liehr, Thomas

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Published in:
Frontiers in molecular neuroscience
Vol. 14 (04.02.2021)
Volume:
14
Date Issued:
04.02.2021
URN:
urn:nbn:de:gbv:27-dbt-20210318-141445-009
DOI:
10.3389/fnmol.2021.613091
Language:
English
Type of Resource:
Text
Extent:
12 Seiten
Place Term:
Lausanne
Publisher:
Frontiers Research Foundation
Keywords:
microcephaly; magnetic resonace imaging (MRI); intellectual disability—genetics *; PRMT8; array comparative genetic hybridization (aCGH)
DDC subject of DNB:
610 Medical sciences Medicine
Hosting institution:
Friedrich-Schiller-Universität Jena, Medizinische Fakultät
Note:
Zweitveröffentlichung

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License Holder: Copyright © 2021 Rincic, Rados, Kopic, Krsnik and Liehr.

Use and reproduction:
This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.