reference/33140710

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/33140710

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
issn	2324-9269
issueIdentifier	8
pageRange	e1313-
publicationName	Molecular Genetics & Genomic Medicine
startingPage	e1313
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f
bibliographicCitation	Liu J, Lin P, Pang J, Jia Z, Peng Y, Xi H, Wu L, Li Z, Wang H. Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome. Mol Genet Genomic Med. 2020 Aug;8(8):e1313. PMID: 32543076; PMCID: PMC7434750.
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date	2020-06-15^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/mgg3.1313 https://pubmed.ncbi.nlm.nih.gov/PMC7434750 https://pubmed.ncbi.nlm.nih.gov/32543076
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/41103 https://portal.issn.org/resource/ISSN/2324-9269
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome
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