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Subject : bone marrow diseases

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Academic Journal

Polyclonal evolution of Fanconi anemia to MDS and AML revealed at single cell resolution.

Authors : Chang, Lixian¹ (AUTHOR); Cui, Zejia² (AUTHOR); Shi, Deyang¹ (AUTHOR)

Source: Experimental Hematology & Oncology. 9/27/2022, Vol. 11 Issue 1, p1-14. 14p.

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Academic Journal

Clinical and hematological aspects in pediatric patients diagnosed with Fanconi anemia – a single-center experience.

Authors : Jercan, Cristina^1,2; Bică, Ana Maria²; Marcu, Andra Daniela²

Source: Pediatru.ro. 2021, Issue 64, p22-28. 7p.

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Academic Journal

Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question.

Authors : Unal, Sule¹ (AUTHOR) ; Chui, David H.K.² (AUTHOR); Gumruk, Fatma¹ (AUTHOR)

Source: Hemoglobin. Aug2015, Vol. 39 Issue 4, p287-289. 3p.

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Academic Journal

Rare cytogenetic abnormalities in acute myeloid leukemia transformed from Fanconi anemia - a case report.

Authors : Hussain, Shabneez¹ ; Adil, Salman Naseem¹

Source: BMC Research Notes. 2013, Vol. 6 Issue 1, p1-4. 4p. 2 Color Photographs, 1 Black and White Photograph.

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Academic Journal

Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology.

Authors : Nicchia, Elena¹; Greco, Chiara²; De Rocco, Daniela¹

Source: Molecular Genetics & Genomic Medicine. Nov2015, Vol. 3 Issue 6, p500-512. 13p.

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Academic Journal

Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.

Authors : de Garibay, Gorka Ruiz¹; Díaz, Avellaneda¹; Gaviña, Belén¹

Source: European Journal of Human Genetics. Aug2013, Vol. 21 Issue 8, p883-886. 4p. 2 Diagrams, 1 Chart.

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Academic Journal

ENHANCED FREQUENCY OF SISTER CHROMATID EXCHANGES INDUCED BY DIEPOXYBUTANE IS SPECIFIC CHARACTERISTIC OF FANCONI ANEMIA CELLULAR PHENOTYPE.

Authors : JOKSIĆ, Ivana¹; PETROVIĆ, Sandra¹; LESKOVAC, Andreja¹

Source: Genetika (0534-0012). 2013, Vol. 45 Issue 2, p393-403. 11p.

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Academic Journal

FANCONI ANEMIA - RARE CAUSE OF PANCYTOPENIA AT CHILD.

Authors : VODĂ, D.¹; DEACONU, A.²; MUŞAT, A. S.²

Source: Bulletin of the Transilvania University of Brasov, Series VI: Medical Sciences. 2012, Vol. 5 Issue 1, p113-118. 6p.

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Academic Journal

A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites.

Authors : de Vries, Yne¹ ; Lwiwski, Nikki^2,3; Levitus, Marieke^1,4

Source: Anemia (20901267). 2012, p1-6. 6p. 1 Diagram, 1 Chart, 1 Map.

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Academic Journal

Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.

Authors : Gille, Johan J. P.¹ ; Floor, Karijn¹; Kerkhoven, Lianne¹

Source: Anemia (20901267). 2012, p1-13. 13p. 4 Charts.

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فلترة النتائج

Polyclonal evolution of Fanconi anemia to MDS and AML revealed at single cell resolution.

Clinical and hematological aspects in pediatric patients diagnosed with Fanconi anemia – a single-center experience.

Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question.

Rare cytogenetic abnormalities in acute myeloid leukemia transformed from Fanconi anemia - a case report.

Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology.

Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.

ENHANCED FREQUENCY OF SISTER CHROMATID EXCHANGES INDUCED BY DIEPOXYBUTANE IS SPECIFIC CHARACTERISTIC OF FANCONI ANEMIA CELLULAR PHENOTYPE.

FANCONI ANEMIA - RARE CAUSE OF PANCYTOPENIA AT CHILD.

A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites.

Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.

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