Literature DB >> 8160763

Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome.

S A Farrell, B A Paes, M E Lewis.   

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Year:  1994        PMID： 8160763     DOI： 10.1002/ajmg.1320500123

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  5 in total

1.  Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene.

Authors:  L Van Maldergem; H A Siitonen; N Jalkh; E Chouery; M De Roy; V Delague; M Muenke; E W Jabs; J Cai; L L Wang; S E Plon; C Fourneau; M Kestilä; Y Gillerot; A Mégarbané; A Verloes
Journal:  J Med Genet       Date:  2005-06-17       Impact factor: 6.318

Review 2.  Baller-Gerold syndrome associated with congenital portal venous malformation.

Authors:  R Savarirayan; P Tomlinson; E Thompson
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

3.  Fetal exposure to sodium valproate associated with Baller-Gerold syndrome: case report and review of the literature.

Authors:  Ricardo Santos de Oliveira; Elizabeth Lajeunie; Eric Arnaud; Dominique Renier
Journal:  Childs Nerv Syst       Date:  2005-03-23       Impact factor: 1.475

4.  Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations.

Authors:  Elisa Adele Colombo; Hatice Mutlu-Albayrak; Yousef Shafeghati; Mine Balasar; Juliette Piard; Davide Gentilini; Anna Maria Di Blasio; Cristina Gervasini; Lionel Van Maldergem; Lidia Larizza
Journal:  Front Pediatr       Date:  2019-05-28       Impact factor: 3.418

5.  Radial, renal and craniofacial anomalies: Baller-Gerold syndrome.

Authors:  Jyotsna Murthy; Ramesh Babu; Padmasani Venkat Ramanan
Journal:  Indian J Plast Surg       Date:  2008-01
  5 in total

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