Disease: Craniosynostosis radial aplasia syndrome
- A further case with Baller-Gerold syndrome (craniosynostosis--radial aplasia syndrome)--overview and new viewpoints on a rare syndrome
- Baller-Gerold Syndrome
- Baller-Gerold syndrome associated with dextrocardia
- Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome
- Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3
- Congenital Malformations Attributed to Prenatal Exposure to Cyclophosphamide
- Correction of the Thumb in Apert Syndrome - Modified Dome Osteotomy and Bilobed Flap
- Cranial vault growth in multiple-suture nonsyndromic and syndromic craniosynostosis: a postoperative long-term anthropometric follow-up
- Craniosynostosis and radial ray defect: a rare presentation of 22q11.2 deletion syndrome
- Craniosynostosis--radial aplasia syndrome
- Human RecQL4 helicase plays multifaceted roles in the genomic stability of normal and cancer cells
- Identification of novel compound heterozygous RECQL4 mutations and prenatal diagnosis of Baller-Gerold syndrome: a case report
- Nationwide survey of Baller‑Gerold syndrome in Japanese population
- Novel FGF9 variant contributes to multiple synostoses syndrome 3
- Open-wedge osteotomy for thumb radial angulation in Apert syndrome using a bone-graft substitute
- Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and <em>ESCO2</em> Mutations
- Phenotypic variability in the Baller-Gerold syndrome: report of a mildly affected patient and review of the literature
- RAPADILINO RECQL4 mutant protein lacks helicase and ATPase activity
- RECQL4 Regulates p53 Function In Vivo During Skeletogenesis
- Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes
- Upper extremity anomalies in Pfeiffer syndrome and mutational correlations