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Deafness, congenital heart defects, and posterior embryotoxon

MedGen UID:
355614
Concept ID:
C1866053
Disease or Syndrome
Synonyms: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
 
OMIM®: 601920

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Le Caignec C, Lefevre M, Schott JJ, Chaventre A, Gayet M, Calais C, Moisan JP
Am J Hum Genet 2002 Jul;71(1):180-6. Epub 2002 May 17 doi: 10.1086/341327. [Epub ahead of print] PMID: 12022040Free PMC Article

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