reference/16657006

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bibliographicCitation	Demirhan O, Türkmen S, Schwabe GC, Soyupak S, Akgül E, Tastemir D, Karahan D, Mundlos S, Lehmann K. A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies. J Med Genet. 2005 Apr;42(4):314–7. PMID: 15805157; PMCID: PMC1736042.
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date	2005-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC1736042 https://pubmed.ncbi.nlm.nih.gov/15805157 https://doi.org/10.1136/jmg.2004.023564
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies
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Total number of triples: 59.