Overlap between Rothmund-Thomson and Baller-Gerold syndrome. | European Journal of Pediatric Dermatology
Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS - ScienceDirect
Baller-Gerold syndrome: MedlinePlus Genetics
Rothmund-Thomson syndrome | Orphanet Journal of Rare Diseases | Full Text
Frontiers | Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations
Baller-Gerold syndrome: MedlinePlus Genetics
The Baller-Gerold syndrome
Clinical features a associated with the Baller-Gerold,... | Download Table
Baller-Gerold Syndrome in a Premature Infant with a Mutation in the <i xmlns="">RECQL4</i> Gene
Syndrome de Baller-Gerold - Dysostoses cranio-faciales, costo-vertébrales, rotuliennes et des extrémités et synostoses
36. Baller-Gerold Syndrome: Description of Pathology - Undergraduate Research
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Ballerâ•'Gerold syndrome associated with congenital hydrocephalus
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What is Baller-Gerold Syndrome?
Rothmund-Thomson Syndrome | CancerIndex
Baller-Gerold Syndrome in a Premature Infant with a Mutation in the <i xmlns="">RECQL4</i> Gene
Radial, renal and craniofacial anomalies: Baller-Gerold syndrome – ScienceOpen
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene | Journal of Medical Genetics
Baller–Gerold syndrome - Wikipedia
Baller-Gerold-Syndrom - DocCheck Flexikon
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene | Journal of Medical Genetics
Baller-Gerold syndrome: MedlinePlus Genetics
A patient with Baller–Gerold syndrome and midline NK/T lymphoma - Debeljak - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Craniosynostosis | European Journal of Human Genetics