125 related articles for article (PubMed ID: 36759292)
1. Clinical and cytogenetic profile of Fanconi anemia diagnosed after implementation of mitomycin C cytogenetic test in the state of Pernambuco, Brazil.
Borges MLRDR; Souza JLC; Rodrigues LH; Cornélio MTMN; Anjos ACD; Santos N; Salles TJM
Hematol Transfus Cell Ther; 2024; 46(2):113-118. PubMed ID: 36759292
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.
Francies FZ; Wainwright R; Poole J; De Leeneer K; Coene I; Wieme G; Poirel HA; Brichard B; Vermeulen S; Vral A; Slabbert J; Claes K; Baeyens A
DNA Repair (Amst); 2018 Jan; 61():17-24. PubMed ID: 29154021
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Cytogenetic findings in Polish patients with suspected Fanconi anemia.
Repczyńska A; Jułga K; Lorenc A; Skalska-Sadowska J; Wysocki M; Zaucha-Prażmo A; Drabko K; Bossowski A; Dembowska-Bagińska B; Wachowiak J; Buciński A; Haus O
Adv Clin Exp Med; 2024 Apr; 33(4):361-368. PubMed ID: 37540155
[TBL] [Abstract][Full Text] [Related]
5. Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.
Behera CK; Gyandeep G; Mishra R; Mohanty RP; Pal A; Behera J; Samal S; Das B
Mol Biol Rep; 2023 Jan; 50(1):931-936. PubMed ID: 36369330
[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. 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]
8. [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]
9. Diagnosis of Fanconi anemia in patients with bone marrow failure.
Pinto FO; Leblanc T; Chamousset D; Le Roux G; Brethon B; Cassinat B; Larghero J; de Villartay JP; Stoppa-Lyonnet D; Baruchel A; Socié G; Gluckman E; Soulier J
Haematologica; 2009 Apr; 94(4):487-95. PubMed ID: 19278965
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Evaluation of concentration and storage effects of mitomycin C in the diagnosis of Fanconi anemia among idiopatic aplastic anemia patients.
Mozdarani H; Ashtiani KA; Mohseni-Meybodi A
Indian J Hum Genet; 2011 Sep; 17(3):145-51. PubMed ID: 22345984
[TBL] [Abstract][Full Text] [Related]
12. An uncommon t(9;11)(p24;q22) with monoallelic loss of
Lovatel VL; de Souza DC; Alvarenga TF; Capela de Matos RR; Diniz C; Schramm MT; Llerena Júnior JC; Silva MLM; Abdelhay E; de Souza Fernandez T
Mol Cytogenet; 2018; 11():40. PubMed ID: 30008805
[TBL] [Abstract][Full Text] [Related]
13. Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.
Doubaj Y; Zrhidri A; Elalaoui SC; Lyahyai J; El Kadiri Y; Elkassimi N; Sbiti A; El Kababri M; Hessissen L; Sefiani A
Pan Afr Med J; 2021; 39():72. PubMed ID: 34422195
[TBL] [Abstract][Full Text] [Related]
14. Functional analysis of Fanconi anemia mutations in China.
Li N; Ding L; Li B; Wang J; D'Andrea AD; Chen J
Exp Hematol; 2018 Oct; 66():32-41.e8. PubMed ID: 30031030
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Chromosomal breakage tests in the differential diagnosis of Fanconi anemia and aplastic anemia.
Farkas G; Székely G; Goda V; Kállay KM; Kocsis ZS; Szakszon K; Benyó G; Erdélyi D; Liptai Z; Csordás K; Kertész G; Szegedi I; Kriván G; Takácsi-Nagy Z; Polgár C; Jurányi Z
Eur J Haematol; 2023 Aug; 111(2):254-262. PubMed ID: 37194391
[TBL] [Abstract][Full Text] [Related]
17. Comprehensive analysis on phenotype and genetic basis of Chinese Fanconi anemia patients: dismal outcomes call for nationwide studies.
Nie D; Zhang J; Wang F; Zhang W; Liu L; Chen X; Zhang Y; Cao P; Xiong M; Wang T; Wu P; Ma X; Tian W; Wang M; Chen KN; Liu H
BMC Med Genet; 2020 Jun; 21(1):118. PubMed ID: 32487094
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Fanconi Anemia: A Rare Genetic Disorder.
Thakur B; Hiwale KM
Cureus; 2023 May; 15(5):e38899. PubMed ID: 37303314
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
