Baller-Gerold Syndrome Latest Advances

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