BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 12557968)

  • 1. Baller-Gerold syndrome.
    Anoop P; Sasidharan CK
    Indian J Pediatr; 2002 Dec; 69(12):1097-8. PubMed ID: 12557968
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Baller-Gerold syndrome associated with congenital portal venous malformation.
    Savarirayan R; Tomlinson P; Thompson E
    J Med Genet; 1998 Sep; 35(9):767-9. PubMed ID: 9733037
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further delineation of the Baller-Gerold syndrome.
    Lin AE; McPherson E; Nwokoro NA; Clemens M; Losken HW; Mulvihill JJ
    Am J Med Genet; 1993 Feb; 45(4):519-24. PubMed ID: 8465861
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome.
    Pelias MZ; Superneau DW; Thurmon TF
    Am J Med Genet; 1981; 10(2):133-9. PubMed ID: 7315870
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mid-portion agenesis of corpus callosum in a presumed Baller-Gerold syndrome.
    Dunac A; Van Bogaert P; David P; Avni EF; Paduart O; Szliwowski HB; Van Regemorter N
    Neuropediatrics; 1995 Oct; 26(5):273-5. PubMed ID: 8552221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Baller-Gerold syndrome].
    Satokata I
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):136-7. PubMed ID: 11057169
    [No Abstract]   [Full Text] [Related]  

  • 7. Baller-Gerold syndrome associated with dextrocardia.
    Ceylan A; Peker E; Dogan M; Tuncer O; Kirimi E
    Genet Couns; 2011; 22(1):69-74. PubMed ID: 21614991
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotypic variability in the Baller-Gerold syndrome: report of a mildly affected patient and review of the literature.
    Ramos Fuentes FJ; Nicholson L; Scott CI
    Eur J Pediatr; 1994 Jul; 153(7):483-7. PubMed ID: 7957363
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Osteosarcoma in a 16-year-old boy with Baller-Gerold syndrome.
    Preis S; Majewski F; Körholz D; Göbel U
    Clin Dysmorphol; 1995 Apr; 4(2):161-8. PubMed ID: 7606324
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome.
    Gripp KW; Stolle CA; Celle L; McDonald-McGinn DM; Whitaker LA; Zackai EH
    Am J Med Genet; 1999 Jan; 82(2):170-6. PubMed ID: 9934984
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Baller-Gerold syndrome: an 11th case of craniosynostosis and radial aplasia.
    Boudreaux JM; Colon MA; Lorusso GD; Parro EA; Pelias MZ
    Am J Med Genet; 1990 Dec; 37(4):447-50. PubMed ID: 2260585
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Craniosynostosis and radial ray defect: a rare presentation of 22q11.2 deletion syndrome.
    Rojnueangnit K; Robin NH
    Am J Med Genet A; 2013 Aug; 161A(8):2024-6. PubMed ID: 23813949
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.
    Rossbach HC; Sutcliffe MJ; Haag MM; Grana NH; Rossi AR; Barbosa JL
    Am J Med Genet; 1996 Jan; 61(1):65-7. PubMed ID: 8741921
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Overlap between Baller-Gerold and Rothmund-Thomson syndrome.
    Mégarbané A; Melki I; Souraty N; Gerbaka J; El Ghouzzi V; Bonaventure J; Mornand A; Loiselet J
    Clin Dysmorphol; 2000 Oct; 9(4):303-5. PubMed ID: 11045594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome.
    Anyane-Yeboa K; Gunning L; Bloom AD
    Clin Genet; 1980 Feb; 17(2):161-6. PubMed ID: 7363501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome.
    Farrell SA; Paes BA; Lewis ME
    Am J Med Genet; 1994 Mar; 50(1):98-9. PubMed ID: 8160763
    [No Abstract]   [Full Text] [Related]  

  • 17. The Baller-Gerold syndrome.
    Van Maldergem L; Verloes A; Lejeune L; Gillerot Y
    J Med Genet; 1992 Apr; 29(4):266-8. PubMed ID: 1583650
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Expanding the phenotypic spectrum of the Baller-Gerold syndrome.
    Temtamy SA; Aglan MS; Nemat A; Eid M
    Genet Couns; 2003; 14(3):299-312. PubMed ID: 14577674
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New syndrome with features overlapping the Baller-Gerold and Roberts syndromes.
    Newbury-Ecob RA; McKeever PA; Gosden C; Young ID
    Clin Dysmorphol; 1993 Apr; 2(2):173-7. PubMed ID: 8281283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Craniosynostosis, microcephaly, hydrancephaly, humero-radial synostosis, and thumb aplasia: a new syndrome?
    Samson G; Gardner JC
    Am J Med Genet; 1996 Jan; 61(2):174-7. PubMed ID: 8669448
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.