date: 2020-10-28T13:53:27Z
pdf:PDFVersion: 1.4
pdf:docinfo:title: Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities
xmp:CreatorTool: Springer
access_permission:can_print_degraded: true
subject: GENETICS in MEDICINE, doi:10.1038/s41436-020-01016-6
pdfa:PDFVersion: A-2b
xmpMM:History:Action: converted
language: EN
dc:format: application/pdf; version=1.4
pdf:docinfo:creator_tool: Springer
access_permission:fill_in_form: true
xmpMM:History:When: 2020-10-27T11:58:11Z
pdf:encrypted: false
dc:title: Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities
modified: 2020-10-28T13:53:27Z
cp:subject: GENETICS in MEDICINE, doi:10.1038/s41436-020-01016-6
xmpMM:History:SoftwareAgent: pdfToolbox
pdf:docinfo:custom:CrossMarkDomains[1]: springer.com
pdf:docinfo:subject: GENETICS in MEDICINE, doi:10.1038/s41436-020-01016-6
xmpMM:History:InstanceID: uuid:85a89e81-c77b-43a2-a83d-eadcfb46ad85
pdf:docinfo:creator: Lot Snijders Blok
meta:author: Arianna Vino
meta:creation-date: 2020-10-27T06:27:29Z
created: 2020-10-27T06:27:29Z
access_permission:extract_for_accessibility: true
Creation-Date: 2020-10-27T06:27:29Z
pdfaid:part: 2
pdf:docinfo:custom:CrossMarkDomains[2]: springerlink.com
pdf:docinfo:custom:doi: 10.1038/s41436-020-01016-6
Author: Arianna Vino
doi: 10.1038/s41436-020-01016-6
pdf:unmappedUnicodeCharsPerPage: 0
dc:description: GENETICS in MEDICINE, doi:10.1038/s41436-020-01016-6
Keywords: FOXP4; de novo variants; neurodevelopmental disorder; speech/language disorder; congenital diaphragmatic hernia
access_permission:modify_annotations: true
dc:creator: Arianna Vino
description: GENETICS in MEDICINE, doi:10.1038/s41436-020-01016-6
dcterms:created: 2020-10-27T06:27:29Z
Last-Modified: 2020-10-28T13:53:27Z
dcterms:modified: 2020-10-28T13:53:27Z
title: Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities
xmpMM:DocumentID: uuid:ae6fd10a-ebfb-41ea-9e53-7798be255e55
Last-Save-Date: 2020-10-28T13:53:27Z
CrossMarkDomains[1]: springer.com
pdf:docinfo:keywords: FOXP4; de novo variants; neurodevelopmental disorder; speech/language disorder; congenital diaphragmatic hernia
pdf:docinfo:modified: 2020-10-28T13:53:27Z
meta:save-date: 2020-10-28T13:53:27Z
Content-Type: application/pdf
X-Parsed-By: org.apache.tika.parser.DefaultParser
creator: Arianna Vino
pdfaid:conformance: B
dc:language: EN
dc:subject: FOXP4; de novo variants; neurodevelopmental disorder; speech/language disorder; congenital diaphragmatic hernia
access_permission:assemble_document: true
xmpTPg:NPages: 9
pdf:charsPerPage: 4367
access_permission:extract_content: true
access_permission:can_print: true
CrossMarkDomains[2]: springerlink.com
meta:keyword: FOXP4; de novo variants; neurodevelopmental disorder; speech/language disorder; congenital diaphragmatic hernia
access_permission:can_modify: true
pdf:docinfo:created: 2020-10-27T06:27:29Z