|1.||Suhasini, Avvaru N: 2 articles (04/2013 - 01/2013)|
|2.||Brosh, Robert M: 2 articles (04/2013 - 01/2013)|
|3.||Mégarbané, A: 2 articles (02/2006 - 10/2000)|
|4.||Wu, Jianhong: 1 article (06/2015)|
|5.||Yang, Tao: 1 article (06/2015)|
|6.||Lu, Linchao: 1 article (06/2015)|
|7.||Harutyunyan, Karine: 1 article (06/2015)|
|8.||Tao, Jianning: 1 article (06/2015)|
|9.||Bae, Yangjin: 1 article (06/2015)|
|10.||Jin, Weidong: 1 article (06/2015)|
01/01/2011 - "We report a 4 year old boy in whom the clinical features of craniosynostosis and bilateral absent thumbs and radii led to a diagnosis of Baller-Gerold syndrome. "
11/01/2009 - "Baller-Gerold syndrome (BGS) is characterized by craniosynostosis and preaxial upper-limb malformations, and it has an autosomal recessive inheritance. "
01/01/2008 - "We report a patient with findings of craniosynostosis and radial aplasia consistent with the diagnosis of the Baller-Gerold syndrome. "
02/01/2006 - "Baller-Gerold syndrome (BGS) is a rare autosomal recessive condition with radial aplasia/hypoplasia and craniosynostosis (OMIM 218600). "
02/01/2006 - "Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene."
|2.||Rothmund-Thomson Syndrome (Syndrome, Rothmund-Thomson)
06/01/2015 - "Rothmund-Thomson syndrome, RAPADILINO, and Baller-Gerold syndrome are rare genetic disorders caused by mutations in the RECQL4 gene. "
01/01/2013 - "RECQL4 mutations can lead to Rothmund-Thomson syndrome, Baller-Gerold syndrome, or RAPADILINO. "
10/01/2000 - "Although this patient was originally diagnosed as having Baller-Gerold syndrome it is more likely that he has Rothmund-Thomson syndrome or a similar disorder. "
04/01/2015 - "RECQL4 mutations are associated with Rothmund Thomson Syndrome (RTS), RAPADILINO Syndrome and Baller-Gerold Syndrome. "
04/01/2013 - "Complex phenotypes are also observed for RECQL4 helicase mutations responsible for Rothmund-Thomson syndrome, Baller-Gerold syndrome, or RAPADILINO. "
09/01/1991 - "We present a new case of the Baller-Gerold syndrome (BGS) in an infant with prenatally apparent severe hydrocephalus, growth retardation, and cardiac and limb abnormalities detected by ultrasound at 26 weeks of gestational age. "
09/01/1991 - "Baller-Gerold syndrome associated with congenital hydrocephalus."
01/02/1996 - "Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome."
01/02/1996 - "Clinical manifestations and chromosome breakage, consistent with Fanconi anemia, in patients with a prior diagnosis of either Baller-Gerold syndrome, reported earlier in one other patient [Farrell et al., 1994: Am J Med Genet 50:98-99], or with VACTERL association with hydrocephalus, recently reported in 3 patients [Toriello et al., 1991: Proc Greenwood Genet Center 11:142; Porteus et al., 1992: Am J Med Genet 43:1032-1034], underline the clinical heterogeneity of Fanconi anemia and raise the question of whether these syndromes are distinct disorders or phenotypic variations of the same disease."
01/02/1996 - "Two brothers with presumed Baller-Gerold syndrome, one of whom was previously diagnosed with the association of vertebral, cardiac, renal, limb anomalies, anal atresia, tracheo-esophageal fistula (VACTERL) association with hydrocephalus, were evaluated for chromosome breakage because of severe thrombo cytopenia in one of them. "
02/01/1980 - "A new case of the Baller-Gerold syndrome is described in a 6 1/2-year-old, black male who presented at birth with bilateral synostoses of the coronal and lambdoidal sutures, bilateral radial aplasia, vertebral anomalies and genito-urinary malformations. "
01/01/2006 - "We report three patients with a history of maternal valproate use during pregnancy who presented with a combination of metopic suture synostosis and upper limb malformations, which could be diagnosed as Baller-Gerold syndrome (BGS). "
|5.||Osteosarcoma (Osteogenic Sarcoma)
04/01/1995 - "Osteosarcoma in a 16-year-old boy with Baller-Gerold syndrome."
04/15/2007 - "Mutations in a human RecQ helicase homologue, RECQL4, have been identified in patients with Type II Rothmund-Thomson syndrome (RTS) with osteosarcoma predisposition, RAPADILINO syndrome, and Baller-Gerold syndrome. "
|4.||Valproic Acid (Valproate, Semisodium)