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A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype-phenotype correlation
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Published in: | American journal of medical genetics. Part A 2023, Vol.191 (3), p.870-877 |
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Main Authors: | , , , , , , |
Format: | Report |
Language: | English |
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container_end_page | 877 |
container_issue | 3 |
container_start_page | 870 |
container_title | American journal of medical genetics. Part A |
container_volume | 191 |
creator | Zunova, Hana Stolfa, Miroslav Kunikova, Tereza Novotna, Drahuse Valkovicova, Radka Štěrbová, Katalin Vlckova, Marketa |
description | |
doi_str_mv | 10.1002/ajmg.a.63085 |
format | report |
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fulltext | fulltext |
identifier | EISSN: 1552-4833 |
ispartof | American journal of medical genetics. Part A, 2023, Vol.191 (3), p.870-877 |
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language | eng |
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source | Wiley-Blackwell Read & Publish Collection |
title | A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype-phenotype correlation |
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