Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities
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Published:2021-03
Issue:3
Volume:23
Page:534-542
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Snijders Blok LotORCID,
Vino Arianna,
den Hoed Joery,
Underhill Hunter R.,
Monteil Danielle,
Li Hong,
Reynoso Santos Francis Jeshira,
Chung Wendy K.,
Amaral Michelle D.,
Schnur Rhonda E.,
Santiago-Sim Teresa,
Si Yue,
Brunner Han G.,
Kleefstra Tjitske,
Fisher Simon E.ORCID
Subject
Genetics (clinical)
Cited by
18 articles.
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4. Replication Study of GWAS-Associated Variants in the <i>TUFM</i>, <i>SH2B1</i>, <i>ZNF638</i>, <i>NEGR1</i>, <i>ATP2A1</i>, <i>EXOC4</i>, and <i>CSE1L</i> Genes and Cognitive Abilities;Генетика;2023-09-01
5. FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia;Journal of Pediatric Genetics;2023-03-28