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Last Updated: 10/31/2025
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Found 10 publications
Severe Phenotype With RECQL4 Syndrome: A Report of Two Cases.
Journal: American journal of medical genetics. Part A
Published: October 09, 2023
Nationwide survey of Baller‑Gerold syndrome in Japanese population.
Journal: Molecular medicine reports
Published: July 19, 2016
Identification of novel compound heterozygous RECQL4 mutations and prenatal diagnosis of Baller-Gerold syndrome: a case report.
Journal: Genetics and molecular research : GMR
Published: May 13, 2015
Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes.
Journal: Clinical genetics
Published: November 12, 2013
Cranial vault growth in multiple-suture nonsyndromic and syndromic craniosynostosis: a postoperative long-term anthropometric follow-up.
Journal: The Journal of craniofacial surgery
Published: May 30, 2013
Craniosynostosis and radial ray defect: a rare presentation of 22q11.2 deletion syndrome.
Journal: American journal of medical genetics. Part A
Published: January 23, 2013
Baller-Gerold syndrome associated with dextrocardia.
Journal: Genetic counseling (Geneva, Switzerland)
Published: May 28, 2011
Baller-Gerold syndrome: Further evidence for association with prenatal exposure to valproate.
Journal: Annals of Indian Academy of Neurology
Published: July 05, 2007
Baller Gerold syndrome and Fanconi anaemia.
Journal: American journal of medical genetics
Published: February 05, 1998
Showing 1-10 of 10
Last Updated: 10/31/2025