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BALLER-GEROLD SYNDROME; BGS
(OMIM ID: 218600 )

Known also as: CRANIOSYNOSTOSIS WITH RADIAL DEFECTS CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME


A number sign (#) is used with this entry because of evidence that Baller-Gerold syndrome is due to mutations in the RECQL4 gene and is part of a clinical spectrum that encompasses Rothmund-Thomson syndrome and RAPADILINO syndrome.


DNA repair proteins related with BALLER-GEROLD SYNDROME; BGS (218600 ) disease:
Last modification of this entry: Oct. 11, 2010.

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