Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene
Rothmund-Thomson Syndrome | CancerIndex
Baller-Gerold-Syndrom - DocCheck Flexikon
PDF] Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate | Semantic Scholar
Baller-Gerold syndrome: MedlinePlus Genetics
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. - Abstract - Europe PMC
Baller-Gerold Syndrome in a Premature Infant with a Mutation in the <i xmlns="">RECQL4</i> Gene
Overlap between Rothmund-Thomson and Baller-Gerold syndrome. | European Journal of Pediatric Dermatology
Related HealthJournals - Craniofacial Abnormalities - StoryMD
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A patient with Baller–Gerold syndrome and midline NK/T lymphoma - Debeljak - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Radial, renal and craniofacial anomalies: Baller-Gerold syndrome – ScienceOpen
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: MedlinePlus Genetics
Fetal exposure to sodium valproate associated with Baller–Gerold syndrome: case report and review of the literature | Child's Nervous System
Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS - ScienceDirect