reference/6800030

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6800030

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't\|Systematic Review
endingPage	1842
issn	2472-1727
issueIdentifier	20
pageRange	1834-1842
publicationName	Birth Defects Research
startingPage	1834
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bibliographicCitation	Sun C, Xu D, Pei Z, Yang L, Qiao Z, Lu W, Luo F, Qiu Z. Separation in genetic pathogenesis of mutations in FBN1‐TB5 region between autosomal dominant acromelic dysplasia and Marfan syndrome. Birth Defects Research. 2020 Oct 08;112(20):1834–42. doi: 10.1002/bdr2.1814.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6433-7994 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_53def5f23b144b509f86b282c94a8953 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_75c38bf758732eb657c44328d1bce1a8 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6025-4801 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a45e0c0f94d0c31f2e9284f073ec913e http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f749cfdca0d90dd1b6d4e4932dc98ecc http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e7fc8bf572ed6e77a03abdfd55d4b420 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d6628525cc9267414d929103cfb0923c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7c9662240c640a8c1f5e0b66b4c36135
date	2020-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/33030311 https://doi.org/10.1002/bdr2.1814
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Separation in genetic pathogenesis of mutations in FBN1‐TB5 region between autosomal dominant acromelic dysplasia and Marfan syndrome
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Total number of triples: 41.