Radial, renal and craniofacial anomalies: Baller-Gerold syndrome – ScienceOpen
Clinical features a associated with the Baller-Gerold,... | Download Table
Baller-Gerold syndrome: MedlinePlus Genetics
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Baller-gerold Syndrome Card, Baller-gerold Syndrome Emergency Card, Baller-gerold Syndrome Medical Card, Baller-gerold Syndrome Alert Card - Etsy
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What is Baller-Gerold Syndrome?
PDF) Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene | André Mégarbané and Valérie Delague - Academia.edu
Baller-Gerold-Syndrom - DocCheck Flexikon
Frontiers | Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations
Baller-Gerold Syndrome | Hereditary Ocular Diseases
Syndrome de Baller-Gerold - Dysostoses cranio-faciales, costo-vertébrales, rotuliennes et des extrémités et synostoses
Rothmund-Thomson syndrome | Orphanet Journal of Rare Diseases | Full Text
Baller-Gerold Syndrome a Rare Cau... preview & related info | Mendeley
Baller-Gerold syndrome: MedlinePlus Genetics
36. Baller-Gerold Syndrome: Description of Pathology - Undergraduate Research
A patient with Baller–Gerold syndrome and midline NK/T lymphoma - Debeljak - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene | Journal of Medical Genetics
![PDF] Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c1f3610ed22b81a790fed02352fcbedb74c4dfdb/2-Figure1-1.png "PDF] Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate | Semantic Scholar")
PDF] Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate | Semantic Scholar
Baller–Gerold syndrome - Wikipedia
Rothmund-Thomson Syndrome | CancerIndex
Baller–Gerold syndrome - Wikipedia
Baller-Gerold Syndrome a Rare Cau... preview & related info | Mendeley
Baller-Gerold Syndrome in a Premature Infant with a Mutation in the <i xmlns="">RECQL4</i> Gene
Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS - ScienceDirect
![PDF] Baller-Gerold syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/308da9016014f36bcc5a0a0e353259b6214243b8/1-Figure1-1.png "PDF] Baller-Gerold syndrome | Semantic Scholar")
PDF] Baller-Gerold syndrome | Semantic Scholar
