55 related articles for article (PubMed ID: 5901871)
1. Chromosome abnormalities in constitutional aplastic anemia.
Bloom GE; Warner S; Gerald PS; Diamond LK
N Engl J Med; 1966 Jan; 274(1):8-14. PubMed ID: 5901871
[No Abstract] [Full Text] [Related]
2. [15q26 deletion syndrome with pure red cell aplastic anemia: a case report].
Zhang QG; Fu WJ; Gong WY; Jin QC
Zhonghua Xue Ye Xue Za Zhi; 2023 Jun; 44(6):523. PubMed ID: 37550214
[No Abstract] [Full Text] [Related]
3. Aplastic Anaemia: Problems of Diagnosis and of Treatment.
Lewis SM
J R Coll Physicians Lond; 1969 Apr; 3(3):253-264. PubMed ID: 30667717
[No Abstract] [Full Text] [Related]
4. Impaired TIP60-mediated H4K16 acetylation accounts for the aberrant chromatin accumulation of 53BP1 and RAP80 in Fanconi anemia pathway-deficient cells.
Renaud E; Barascu A; Rosselli F
Nucleic Acids Res; 2016 Jan; 44(2):648-56. PubMed ID: 26446986
[TBL] [Abstract][Full Text] [Related]
5. Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.
Evdokimova VN; McLoughlin RK; Wenger SL; Grant SG
Am J Med Genet A; 2005 May; 135(1):59-65. PubMed ID: 15822129
[TBL] [Abstract][Full Text] [Related]
6. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
Yamashita T; Nakahata T
Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
[TBL] [Abstract][Full Text] [Related]
7. Fanconi anemia.
Basu S; Garewal G; Kaur S; Trehan A; Marwaha RK
Indian J Pediatr; 1996; 63(3):399-402. PubMed ID: 10830019
[No Abstract] [Full Text] [Related]
8. Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly.
Tommerup N; Mortensen E; Nielsen MH; Wegner RD; Schindler D; Mikkelsen M
Hum Genet; 1993 Oct; 92(4):339-46. PubMed ID: 7693575
[TBL] [Abstract][Full Text] [Related]
9. Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cells.
Nordenson I; Björksten B; Lundh B
Hum Genet; 1980; 56(2):169-71. PubMed ID: 7450773
[TBL] [Abstract][Full Text] [Related]
10. Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics.
Mutchinick O; Ruz L; Gonsebatt ME; Mauleón P; Lisker R; García G
Hum Genet; 1981; 59(2):137-40. PubMed ID: 7327573
[TBL] [Abstract][Full Text] [Related]
11. A case of pure red cell aplasia with a high incidence of spontaneous chromosome breakage: a possible X-ray sensitive syndrome.
Iskandar O; Jager MJ; Willenze R; Natarajan AT
Hum Genet; 1980; 55(3):337-40. PubMed ID: 7203468
[TBL] [Abstract][Full Text] [Related]
12. Prenatal recognition of a defect in DNA repair.
Hirsch-Kauffmann M; Schweiger M
Mol Gen Genet; 1981; 184(1):17-9. PubMed ID: 6950194
[No Abstract] [Full Text] [Related]
13. The identification of fanconi anemia genotypes by clastogenic stress.
Cohen MM; Simpson SJ; Honig GR; Maurer HS; Nicklas JW; Martin AO
Am J Hum Genet; 1982 Sep; 34(5):794-810. PubMed ID: 6812413
[TBL] [Abstract][Full Text] [Related]
14. Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage.
Helmerhorst FM; Heaton DC; Crossen PE; von dem Borne AE; Engelfriet CP; Natarajan AT
Hum Genet; 1984; 65(3):252-6. PubMed ID: 6421717
[TBL] [Abstract][Full Text] [Related]
15. Unusual response to bifunctional alkylating agents in a case of Fanconi anaemia.
Kwee ML; Poll EH; van de Kamp JJ; de Koning H; Eriksson AW; Joenje H
Hum Genet; 1983; 64(4):384-7. PubMed ID: 6413386
[TBL] [Abstract][Full Text] [Related]
16. Proliferative kinetics and mitomycin C-induced chromosome damage in Fanconi's anemia lymphocytes.
Miura K; Morimoto K; Koizumi A
Hum Genet; 1983; 63(1):19-23. PubMed ID: 6403454
[TBL] [Abstract][Full Text] [Related]
17. Constitutional aplastic anaemia: a family with a new X linked variety of amegakaryocytic thrombocytopenia.
Griffiths AD
J Med Genet; 1983 Oct; 20(5):361-4. PubMed ID: 6196483
[TBL] [Abstract][Full Text] [Related]
18. [Cytogenetic finding and etiology of Fanconi's anemia. A case of Fanconi's anemia without hexokinase deficiency].
Schroeder TM
Humangenetik; 1966; 3(1):76-81. PubMed ID: 5986057
[No Abstract] [Full Text] [Related]
19. [Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].
Schroeder TM
Humangenetik; 1966; 2(3):287-316. PubMed ID: 5984971
[No Abstract] [Full Text] [Related]
20. Fanconi's anemia. Report of 3 cases.
Ahuja BK; Jain AM; Sethi AS
Indian J Pediatr; 1969 Aug; 36(259):284-90. PubMed ID: 5823633
[No Abstract] [Full Text] [Related]
[Next] [New Search]