Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS - ScienceDirect
Baller-Gerold Syndrome in a Premature Infant with a Mutation in the <i xmlns="">RECQL4</i> Gene
Baller-Gerold syndrome. Craniosynostosis with metopic ridge and radial... | Download Scientific Diagram
Baller-Gerold syndrome. Craniosynostosis with metopic ridge and radial... | Download Scientific Diagram
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Baller-Gerold Sendromu Nedir? - Evrim Ağacı
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Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. - Abstract - Europe PMC
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene
Baller-Gerold Syndrome in a Premature Infant with a Mutation in the <i xmlns="">RECQL4</i> Gene