171 related articles for article (PubMed ID: 36071913)
1. A Narrative Review on Fanconi Anemia: Genetic and Diagnostic Considerations.
Sharma P; Sharma N; Sharma D
Glob Med Genet; 2022 Sep; 9(3):237-241. PubMed ID: 36071913
[TBL] [Abstract][Full Text] [Related]
2. Fanconi anemia presenting as an "evolving" acute leukemia-diagnostic challenges.
Sinha S; Bhargava M
Indian J Med Paediatr Oncol; 2013 Oct; 34(4):305-8. PubMed ID: 24604962
[TBL] [Abstract][Full Text] [Related]
3. Fanconi Anemia: A Rare Genetic Disorder.
Thakur B; Hiwale KM
Cureus; 2023 May; 15(5):e38899. PubMed ID: 37303314
[TBL] [Abstract][Full Text] [Related]
4. [Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report].
Puchmajerová A; Švojgr K; Novotná D; Macháčková E; Sumerauer D; Smíšek P; Kodet R; Kynčl M; Křepelová A; Foretová L
Klin Onkol; 2016; 29 Suppl 1():S89-92. PubMed ID: 26691948
[TBL] [Abstract][Full Text] [Related]
5. Novel
Repczynska A; Pastorczak A; Babol-Pokora K; Skalska-Sadowska J; Drozniewska M; Mlynarski W; Haus O
Mol Cytogenet; 2020; 13():33. PubMed ID: 32793304
[TBL] [Abstract][Full Text] [Related]
6. A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report.
Zareifar S; Dastsooz H; Shahriari M; Faghihi MA; Shekarkhar G; Bordbar M; Zekavat OR; Shakibazad N
BMC Med Genet; 2019 Jul; 20(1):122. PubMed ID: 31288759
[TBL] [Abstract][Full Text] [Related]
7. Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry.
Auerbach AD; Allen RG
Cancer Genet Cytogenet; 1991 Jan; 51(1):1-12. PubMed ID: 1984836
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Myelodysplastic Syndrome, Acute Myeloid Leukemia, and Cancer Surveillance in Fanconi Anemia.
Savage SA; Walsh MF
Hematol Oncol Clin North Am; 2018 Aug; 32(4):657-668. PubMed ID: 30047418
[TBL] [Abstract][Full Text] [Related]
10. An experience with 124 cases of fanconi anemia: clinical spectrum, hematological parameters and chromosomal breakage analysis.
Mahmood R; Mahmood A; Khan SA; Jaffar R
Am J Blood Res; 2021; 11(5):498-503. PubMed ID: 34824882
[TBL] [Abstract][Full Text] [Related]
11. NK Cell Development and Function in Patients with Fanconi Anemia.
Hashemi E; Bjorgaard S; Wang D; Uyemura B; Riese M; Thakar MS; Malarkannan S
Crit Rev Immunol; 2021; 41(2):35-44. PubMed ID: 34348001
[TBL] [Abstract][Full Text] [Related]
12. The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry.
Giampietro PF; Adler-Brecher B; Verlander PC; Pavlakis SG; Davis JG; Auerbach AD
Pediatrics; 1993 Jun; 91(6):1116-20. PubMed ID: 8502512
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A functionally active retrovirus vector for gene therapy in Fanconi anemia group C.
Walsh CE; Grompe M; Vanin E; Buchwald M; Young NS; Nienhuis AW; Liu JM
Blood; 1994 Jul; 84(2):453-9. PubMed ID: 7517716
[TBL] [Abstract][Full Text] [Related]
16. Fanconi anemia: causes and consequences of genetic instability.
Kalb R; Neveling K; Nanda I; Schindler D; Hoehn H
Genome Dyn; 2006; 1():218-242. PubMed ID: 18724063
[TBL] [Abstract][Full Text] [Related]
17. Acute myeloid leukemia in Turkish children with Fanconi anemia. One center experience in the period between 1964-1995.
Gözdaşoğlu S; Ertem M; Uysal Z; Babacan E; Yüksel M; Bökesoy I; Sunguroğlu A; Arcasoy A; Çavdar A
Turk J Haematol; 2009 Sep; 26(3):118-22. PubMed ID: 27265494
[TBL] [Abstract][Full Text] [Related]
18. Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients.
Freire BL; Homma TK; Funari MFA; Lerario AM; Leal AM; Velloso EDRP; Malaquias AC; Jorge AAL
Eur J Med Genet; 2018 Mar; 61(3):130-133. PubMed ID: 29133208
[TBL] [Abstract][Full Text] [Related]
19. [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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]