214 related articles for article (PubMed ID: 8741921)
1. 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]
2. VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
Porteous ME; Cross I; Burn J
Am J Med Genet; 1992 Aug; 43(6):1032-4. PubMed ID: 1415330
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.
Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D
Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240
[TBL] [Abstract][Full Text] [Related]
5. Is there a Baller-Gerold syndrome?
Cohen MM; Toriello HV
Am J Med Genet; 1996 Jan; 61(1):63-4. PubMed ID: 8741920
[No Abstract] [Full Text] [Related]
6. Absence of excess chromosome breakage in a patient with VACTERL-hydrocephalus.
Evans JA; Chodirker BN
Am J Med Genet; 1993 Aug; 47(1):112-3. PubMed ID: 8240537
[No Abstract] [Full Text] [Related]
7. 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]
8. 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]
9. [Vater or Vacterl syndrome (author's transl)].
Baumann W; Greinacher I; Emmrich P; Spranger J
Klin Padiatr; 1976 Jul; 188(4):328-37. PubMed ID: 988425
[TBL] [Abstract][Full Text] [Related]
10. Baller Gerold syndrome and Fanconi anaemia.
Quarrell OW; Maltby EL; Harrison CJ
Am J Med Genet; 1998 Jan; 75(2):228-9. PubMed ID: 9450894
[No Abstract] [Full Text] [Related]
11. 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]
12. Monozygotic twin girls with congenital malformations resembling fanconi anemia.
Poole SR; Smith AC; Hays T; McGavran L; Auerbach AD
Am J Med Genet; 1992 Apr; 42(6):780-4. PubMed ID: 1554014
[TBL] [Abstract][Full Text] [Related]
13. Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS.
Alter BP; Giri N
Am J Med Genet A; 2016 Jun; 170(6):1520-4. PubMed ID: 27028275
[TBL] [Abstract][Full Text] [Related]
14. [Baller-Gerold syndrome].
Satokata I
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):136-7. PubMed ID: 11057169
[No Abstract] [Full Text] [Related]
15. 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]
16. A case of Baller-Gerold syndrome.
Markose G; Fairhurst J; Temple IK
Clin Dysmorphol; 1999 Jan; 8(1):69-71. PubMed ID: 10327256
[No Abstract] [Full Text] [Related]
17. X-linked VACTERL with hydrocephalus: the VACTERL-H syndrome.
Genuardi M; Chiurazzi P; Capelli A; Neri G
Birth Defects Orig Artic Ser; 1993; 29(1):235-41. PubMed ID: 8280876
[No Abstract] [Full Text] [Related]
18. Another TWIST on Baller-Gerold syndrome.
Seto ML; Lee SJ; Sze RW; Cunningham ML
Am J Med Genet; 2001 Dec; 104(4):323-30. PubMed ID: 11754069
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Bronchial anomalies in VACTERL association.
Kanu A; Tegay D; Scriven R
Pediatr Pulmonol; 2008 Sep; 43(9):930-2. PubMed ID: 18671276
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
