258 related articles for article (PubMed ID: 20881871)
1. Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population.
Korgaonkar S; Ghosh K; Jijina F; Vundinti BR
J Pediatr Hematol Oncol; 2010 Nov; 32(8):606-10. PubMed ID: 20881871
[TBL] [Abstract][Full Text] [Related]
2. Differentiation of Fanconi anemia from idiopathic aplastic anemia by induced chromosomal breakage study using mitomycin-C (MMC).
Talwar R; Choudhry VP; Kucheria K
Indian Pediatr; 2004 May; 41(5):473-7. PubMed ID: 15181297
[TBL] [Abstract][Full Text] [Related]
3. Differentiation of Fanconi anemia and aplastic anemia using mitomycin C test in Tunisia.
Talmoudi F; Kilani O; Ayed W; Ben Halim N; Mellouli F; Torjmane L; Aissaoui L; Ben Youssef Y; Kammoun L; Ben Othmane T; Bejaoui M; Ben Romdhane N; Elloumi M; Hadiji S; Hentati S; Chemkhi I; Abidli N; Guermani H; Abdelhak S; Amouri A
C R Biol; 2013 Jan; 336(1):29-33. PubMed ID: 23537767
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia.
Talmoudi F; Kammoun L; Benhalim N; Torjemane L; Ouederni M; Aissaoui L; Lakhal A; Mellouli F; Othmen TB; Bejaoui M; Abdelhak S; Meddeb M; Dellagi K; Hdiji S; Amouri A;
J Pediatr Hematol Oncol; 2013 Oct; 35(7):547-50. PubMed ID: 23337544
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Correlation of single-cell gel electrophoresis and mitomycin C-induced chromosomal breakage for chromosomal instabiligy in children with Fanconi anemia].
Zhang L; Liu Q; Zou Y; Liu XM; Zhang JY; Wang SC; Chen XJ; Guo Y; Yang WY; Ruan M; Liu TF; Liu F; Cai XJ; Chen YM; Zhu XF
Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):122-5. PubMed ID: 23527978
[TBL] [Abstract][Full Text] [Related]
7. Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia.
Cervenka J; Arthur D; Yasis C
Pediatrics; 1981 Jan; 67(1):119-27. PubMed ID: 7243420
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Identification of a novel large intragenic deletion in a family with Fanconi anemia: first molecular report from India and review of literature.
Shukla P; Rao A; Ghosh K; Vundinti BR
Gene; 2013 Apr; 518(2):470-5. PubMed ID: 23370339
[TBL] [Abstract][Full Text] [Related]
10. Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes.
Fargo JH; Rochowski A; Giri N; Savage SA; Olson SB; Alter BP
Cytogenet Genome Res; 2014; 144(1):15-27. PubMed ID: 25227706
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.
Auerbach AD; Adler B; Chaganti RS
Pediatrics; 1981 Jan; 67(1):128-35. PubMed ID: 7243421
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic investigation in Iranian patients suspected with Fanconi anemia.
Tootian S; Mahjoubi F; Rahnama M; Hormozian F; Mortezapour F; Razazian F; Manoochehri F; Zamanian M; Nasiri F; Soleymani S; Seyedmortaz L
J Pediatr Hematol Oncol; 2006 Dec; 28(12):834-6. PubMed ID: 17164655
[TBL] [Abstract][Full Text] [Related]
14. Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia.
Auerbach AD; Min Z; Ghosh R; Pergament E; Verlinsky Y; Nicolas H; Boué J
Hum Genet; 1986 May; 73(1):86-8. PubMed ID: 3458668
[TBL] [Abstract][Full Text] [Related]
15. The clinical and biological overlap between Nijmegen Breakage Syndrome and Fanconi anemia.
Gennery AR; Slatter MA; Bhattacharya A; Barge D; Haigh S; O'Driscoll M; Coleman R; Abinun M; Flood TJ; Cant AJ; Jeggo PA
Clin Immunol; 2004 Nov; 113(2):214-9. PubMed ID: 15451479
[TBL] [Abstract][Full Text] [Related]
16. FANCD2 Western blot as a diagnostic tool for Brazilian patients with Fanconi anemia.
Pilonetto DV; Pereira NF; Bitencourt MA; Magdalena NI; Vieira ER; Veiga LB; Cavalli IJ; Ribeiro RC; Pasquini R
Braz J Med Biol Res; 2009 Mar; 42(3):237-43. PubMed ID: 19287902
[TBL] [Abstract][Full Text] [Related]
17. A novel diagnostic screen for defects in the Fanconi anemia pathway.
Shimamura A; Montes de Oca R; Svenson JL; Haining N; Moreau LA; Nathan DG; D'Andrea AD
Blood; 2002 Dec; 100(13):4649-54. PubMed ID: 12393398
[TBL] [Abstract][Full Text] [Related]
18. Fanconi's anemia: the preanemic phase.
McIntosh S; Breg WR; Lubiniecki AS
Am J Pediatr Hematol Oncol; 1979; 1(2):107-10. PubMed ID: 94509
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Severe telomere shortening in Fanconi anemia complementation group L.
Shah A; George M; Dhangar S; Rajendran A; Mohan S; Vundinti BR
Mol Biol Rep; 2021 Jan; 48(1):585-593. PubMed ID: 33394227
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
