262 related articles for article (PubMed ID: 21514743)
1. Incidence of Fanconi anemia in children with congenital thumb anomalies referred for diepoxybutane testing.
Webb ML; Rosen H; Taghinia A; McCarty ER; Cerrato F; Upton J; Labow BI
J Hand Surg Am; 2011 Jun; 36(6):1052-7. PubMed ID: 21514743
[TBL] [Abstract][Full Text] [Related]
2. Fanconi's anaemia and unilateral thumb polydactyly--don't miss it.
Wilks DJ; Kay SP; Bourke G
J Plast Reconstr Aesthet Surg; 2012 Aug; 65(8):1083-6. PubMed ID: 22386531
[TBL] [Abstract][Full Text] [Related]
3. The incidence and spectrum of congenital hand differences in patients with Fanconi anaemia: analysis of 48 patients.
Bourke G; Wilks D; Kinsey S; Feltbower RG; Giri N; Alter BP
J Hand Surg Eur Vol; 2022 Jul; 47(7):711-715. PubMed ID: 35360980
[TBL] [Abstract][Full Text] [Related]
4. DEB test for Fanconi anemia detection in patients with atypical phenotypes.
Esmer C; Sánchez S; Ramos S; Molina B; Frias S; Carnevale A
Am J Med Genet A; 2004 Jan; 124A(1):35-9. PubMed ID: 14679584
[TBL] [Abstract][Full Text] [Related]
5. Fanconi anemia screening by diepoxybutane and mitomicin C tests in Korean children with bone marrow failure syndromes.
Kook H; Cho D; Cho SH; Hong WP; Kim CJ; Park JY; Yoon WS; Ryang DW; Hwang TJ
J Korean Med Sci; 1998 Dec; 13(6):623-8. PubMed ID: 9886171
[TBL] [Abstract][Full Text] [Related]
6. Fanconi anemia with concurrent thumb polydactyly and dorsal dimelia: a case report with discussion of embryology.
Al-Qattan MM
Ann Plast Surg; 2013 Jan; 70(1):116-8. PubMed ID: 21862914
[TBL] [Abstract][Full Text] [Related]
7. New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia.
Giampietro PF; Auerbach AD; Elias ER; Gutman A; Zellers NJ; Davis JG
Am J Med Genet; 1998 Jun; 78(1):70-5. PubMed ID: 9637428
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience.
Altay C; Alikaşifoglu M; Kara A; Tunçbilek E; Ozbek N; Schroeder-Kurth TM
Clin Genet; 1997 May; 51(5):296-302. PubMed ID: 9212176
[TBL] [Abstract][Full Text] [Related]
10. Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane.
Deviren A; Yalman N; Hacihanefioglu S
Ann Hematol; 2003 Apr; 82(4):223-7. PubMed ID: 12707724
[TBL] [Abstract][Full Text] [Related]
11. Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population.
Korgaonkar S; Ghosh K; Vundinti BR
Hematology; 2010 Feb; 15(1):58-62. PubMed ID: 20132664
[TBL] [Abstract][Full Text] [Related]
12. Characteristics of patients with hypoplastic thumb: a prospective study of 51 patients with the results of surgical treatment.
Abdel-Ghani H; Amro S
J Pediatr Orthop B; 2004 Mar; 13(2):127-38. PubMed ID: 15076593
[TBL] [Abstract][Full Text] [Related]
13. Fanconi anemia with cleft palate.
Jurca A; Kinga K; Bembea M; Gug C; Jurca C
Rev Med Chir Soc Med Nat Iasi; 2014; 118(4):1074-7. PubMed ID: 25581972
[TBL] [Abstract][Full Text] [Related]
14. [Fanconi anemia: cytogenetic diagnosis of 40 cases].
Porto B; Sousa R; Ponte F; Torgal A; Campilho F; Campos A; Gonçalves C; Barbot J
Acta Med Port; 2011; 24(3):405-12. PubMed ID: 22015027
[TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalities.
Hurst JA; Baraitser M; Wonke B
Am J Med Genet; 1991 Sep; 40(4):482-4. PubMed ID: 1746615
[TBL] [Abstract][Full Text] [Related]
16. Diagnosis of Fanconi anemia by diepoxybutane analysis.
Auerbach AD
Curr Protoc Hum Genet; 2015 Apr; 85():8.7.1-8.7.17. PubMed ID: 25827349
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage test.
Hou JW; Wang TR
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(2):121-6. PubMed ID: 9151465
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic differentiation of Fanconi anemia, "idiopathic" aplastic anemia, and Fanconi anemia heterozygotes.
Cervenka J; Hirsch BA
Am J Med Genet; 1983 Jun; 15(2):211-23. PubMed ID: 6410915
[TBL] [Abstract][Full Text] [Related]
20. Heterogeneous Diagnoses Underlying Radial Ray Anomalies.
Sevilla-Montoya R; Aguinaga M; Martínez A; Razo G; Molina B; Frías S; Grether P
Indian J Pediatr; 2017 Mar; 84(3):200-205. PubMed ID: 27987078
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
