Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01734.x/fullpdf
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4. Lethal osteochondrodysplasias: prenatal and postnatal differential diagnosis.;Sauer;Ultraschall Med,2000
5. Fetal fibrochondrogenesis at 26 weeks' gestation.;Randrianaivo;Prenat Diagn,2002
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