Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS - ScienceDirect
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 syndrome. Craniosynostosis with metopic ridge and radial... | Download Scientific Diagram
![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
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What is Baller-Gerold Syndrome?
36. Baller-Gerold Syndrome: Description of Pathology - Undergraduate Research
![PDF] Fetal sodium valproate exposure causes Baller-Gerold syndrome phenotype: both phenotypes in the same family. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/14155f5f0564197289dc6a0ca5c2c6caffe4f455/2-Figure1-1.png "PDF] Fetal sodium valproate exposure causes Baller-Gerold syndrome phenotype: both phenotypes in the same family. | Semantic Scholar")
PDF] Fetal sodium valproate exposure causes Baller-Gerold syndrome phenotype: both phenotypes in the same family. | Semantic Scholar
Baller-Gerold Syndrome - StoryMD
The Baller-Gerold syndrome
Radial, renal and craniofacial anomalies: Baller-Gerold syndrome – ScienceOpen
Baller-Gerold syndrome: MedlinePlus Genetics
![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
Baller-Gerold Sendromu Nedir? - Evrim Ağacı
A patient with Baller–Gerold syndrome and midline NK/T lymphoma - Debeljak - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF) Roberts syndrome as a phenocopy of Baller-Gerold syndrome in two patients with craniosynostosis, tetraphocomelia and ESCO2 mutations
Syndrome de Baller-Gerold - Dysostoses cranio-faciales, costo-vertébrales, rotuliennes et des extrémités et synostoses
Baller-Gerold syndrome: MedlinePlus Genetics
36. Baller-Gerold Syndrome: Description of Pathology - Undergraduate Research
The versatile RECQL4 | Genetics in Medicine
EPOS™
Nationwide survey of Baller‑Gerold syndrome in Japanese population
Rothmund-Thomson syndrome | Orphanet Journal of Rare Diseases | Full Text
Baller–Gerold syndrome - Wikipedia
36. Baller-Gerold Syndrome: Description of Pathology - Undergraduate Research
Craniosynostosis | European Journal of Human Genetics
