155 related articles for article (PubMed ID: 433924)
1. Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods.
Auerbach AD; Warburton D; Bloom AD; Chaganti RS
Am J Hum Genet; 1979 Jan; 31(1):77-81. PubMed ID: 433924
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Prenatal diagnosis of Fanconi anemia.
Voss R; Kohn G; Shaham M; Benzur Z; Arnon J; Ornoy A; Yaffe H; Golbus M; Auerbach AD
Clin Genet; 1981 Sep; 20(3):185-90. PubMed ID: 7307316
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemia.
Shipley J; Rodeck CH; Garrett C; Galbraith J; Giannelli F
Prenat Diagn; 1984; 4(3):217-21. PubMed ID: 6431403
[TBL] [Abstract][Full Text] [Related]
7. Fanconi's anemia--chromosome breakage studies in homozygotes and heterozygotes.
Rosendorff J; Bernstein R
Cancer Genet Cytogenet; 1988 Jul; 33(2):175-83. PubMed ID: 3133104
[TBL] [Abstract][Full Text] [Related]
8. Monitoring of pregnancies at risk for Fanconi's anemia by chorionic villi sampling.
Dallapiccola B; Doria Lamba Carbone L; Ferranti G; Cristiani ML; Dagna Bricarelli F
Acta Haematol; 1985; 73(3):157-8. PubMed ID: 3929530
[TBL] [Abstract][Full Text] [Related]
9. Fanconi anemia: prenatal diagnosis in 30 fetuses at risk.
Auerbach AD; Sagi M; Adler B
Pediatrics; 1985 Nov; 76(5):794-800. PubMed ID: 4058989
[TBL] [Abstract][Full Text] [Related]
10. Diagnosis of fanconi anemia by diepoxybutane analysis.
Auerbach AD
Curr Protoc Hum Genet; 2003 Jul; Chapter 8():Unit 8.7. PubMed ID: 18428345
[TBL] [Abstract][Full Text] [Related]
11. Chromosome breakage in Fanconi's anemia and normal cells following in vitro and in vivo cocultivation.
Shaham M; Adler B
Cancer Genet Cytogenet; 1986 Dec; 23(4):315-20. PubMed ID: 3536074
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Transfection of normal human and Chinese hamster DNA corrects diepoxybutane-induced chromosomal hypersensitivity of Fanconi anemia fibroblasts.
Shaham M; Adler B; Ganguly S; Chaganti RS
Proc Natl Acad Sci U S A; 1987 Aug; 84(16):5853-7. PubMed ID: 3475705
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Fanconi's anemia: a cytogenetic study on lymphocyte and bone marrow cultures utilizing 1,2:3,4-diepoxybutane.
Marx MP; Smith S; Heyns AD; van Tonder IZ
Cancer Genet Cytogenet; 1983 May; 9(1):51-9. PubMed ID: 6839306
[TBL] [Abstract][Full Text] [Related]
17. Effect of oxidants and antioxidants on chromosomal breakage in Fanconi anemia lymphocytes.
Dallapiccola B; Porfirio B; Mokini V; Alimena G; Isacchi G; Gandini E
Hum Genet; 1985; 69(1):62-5. PubMed ID: 3967890
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes.
Porfirio B; Dallapiccola B; Mokini V; Alimena G; Gandini E
Hum Genet; 1983; 63(2):117-20. PubMed ID: 6840755
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
