BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 27041517)

  • 41. 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]  

  • 42. Common Variable Immunodeficiency Caused by FANC Mutations.
    Sekinaka Y; Mitsuiki N; Imai K; Yabe M; Yabe H; Mitsui-Sekinaka K; Honma K; Takagi M; Arai A; Yoshida K; Okuno Y; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Muramatsu H; Kojima S; Hira A; Takata M; Ohara O; Ogawa S; Morio T; Nonoyama S
    J Clin Immunol; 2017 Jul; 37(5):434-444. PubMed ID: 28493158
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.
    De Rocco D; Bottega R; Cappelli E; Cavani S; Criscuolo M; Nicchia E; Corsolini F; Greco C; Borriello A; Svahn J; Pillon M; Mecucci C; Casazza G; Verzegnassi F; Cugno C; Locasciulli A; Farruggia P; Longoni D; Ramenghi U; Barberi W; Tucci F; Perrotta S; Grammatico P; Hanenberg H; Della Ragione F; Dufour C; Savoia A;
    Haematologica; 2014 Jun; 99(6):1022-31. PubMed ID: 24584348
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Molecular and prenatal diagnosis of a family with Fanconi anemia by next generation sequencing].
    Gong Z; Yu Y; Zhang Q; Gu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):204-7. PubMed ID: 25863087
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Investigation of FANCA gene in Fanconi anaemia patients in Iran.
    Moghadam AA; Mahjoubi F; Reisi N; Vosough P
    Indian J Med Res; 2016 Feb; 143(2):184-96. PubMed ID: 27121516
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes.
    Flynn EK; Kamat A; Lach FP; Donovan FX; Kimble DC; Narisu N; Sanborn E; Boulad F; Davies SM; Gillio AP; Harris RE; MacMillan ML; Wagner JE; Smogorzewska A; Auerbach AD; Ostrander EA; Chandrasekharappa SC
    Hum Mutat; 2014 Nov; 35(11):1342-53. PubMed ID: 25168418
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation.
    Shamseldin HE; Elfaki M; Alkuraya FS
    J Med Genet; 2012 Mar; 49(3):184-6. PubMed ID: 22232082
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Diagnosis status and genetic characteristics analysis of Fanconi anemia in China].
    Li N; Hu DX; Qin X; Zhu YP; Zhou M; He L; Chang LX; Xu XJ; Dai Y; Cao XY; Chen K; Wang HM; Wang CJ; He YL; Qian XW; Xu LP; Chen J
    Zhonghua Er Ke Za Zhi; 2023 Oct; 61(10):889-895. PubMed ID: 37803855
    [No Abstract]   [Full Text] [Related]  

  • 49. Fanconi anemia: genetic testing in Ashkenazi Jews.
    Auerbach AD
    Genet Test; 1997; 1(1):27-33. PubMed ID: 10464622
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group.
    Fu KL; Thuss PC; Fujino T; Digweed M; Liu JM; Walsh CE
    Hum Genet; 1998 Feb; 102(2):166-9. PubMed ID: 9521584
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Fanconi anemia: current management.
    Kook H
    Hematology; 2005; 10 Suppl 1():108-10. PubMed ID: 16188650
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Novel Variations of FANCA Gene Provokes Fanconi Anemia: Molecular Diagnosis in a Special Chinese Family.
    Li N; Song A; Ding L; Zhu H; Li G; Miao Y; Wang J; Li B; Chen J
    J Pediatr Hematol Oncol; 2018 Jul; 40(5):e299-e304. PubMed ID: 29702541
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Frequency of Fanconi anemia in Brazil and efficacy of screening for the FANCA 3788-3790del mutation.
    Magdalena N; Pilonetto DV; Bitencourt MA; Pereira NF; Ribeiro RC; Jeng M; Pasquini R
    Braz J Med Biol Res; 2005 May; 38(5):669-73. PubMed ID: 15917947
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.
    Gross M; Hanenberg H; Lobitz S; Friedl R; Herterich S; Dietrich R; Gruhn B; Schindler D; Hoehn H
    Cytogenet Genome Res; 2002; 98(2-3):126-35. PubMed ID: 12697994
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.
    Mori M; Hira A; Yoshida K; Muramatsu H; Okuno Y; Shiraishi Y; Anmae M; Yasuda J; Tadaka S; Kinoshita K; Osumi T; Noguchi Y; Adachi S; Kobayashi R; Kawabata H; Imai K; Morio T; Tamura K; Takaori-Kondo A; Yamamoto M; Miyano S; Kojima S; Ito E; Ogawa S; Matsuo K; Yabe H; Yabe M; Takata M
    Haematologica; 2019 Oct; 104(10):1962-1973. PubMed ID: 30792206
    [TBL] [Abstract][Full Text] [Related]  

  • 56. From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.
    Krausz C; Riera-Escamilla A; Chianese C; Moreno-Mendoza D; Ars E; Rajmil O; Pujol R; Bogliolo M; Blanco I; Rodríguez I; Badell I; Ruiz-Castañé E; Surrallés J
    Genet Med; 2019 Jan; 21(1):189-194. PubMed ID: 29904161
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Validation of Fanconi anemia complementation Group A assignment using molecular analysis.
    Moghrabi NN; Johnson MA; Yoshitomi MJ; Zhu X; Al-Dhalimy MJ; Olson SB; Grompe M; Richards CS
    Genet Med; 2009 Mar; 11(3):183-92. PubMed ID: 19367192
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Fanconi anemia in Ashkenazi Jews.
    Kutler DI; Auerbach AD
    Fam Cancer; 2004; 3(3-4):241-8. PubMed ID: 15516848
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant.
    Savino M; Borriello A; D'Apolito M; Criscuolo M; Del Vecchio M; Bianco AM; Di Perna M; Calzone R; Nobili B; Zatterale A; Zelante L; Joenje H; Della Ragione F; Savoia A
    Hum Mutat; 2003 Oct; 22(4):338-9. PubMed ID: 12955722
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes.
    Farah RA; Nair P; Koueik J; Yammine T; Khalifeh H; Korban R; Collet A; Khayat C; Dubois-Denghien C; Chouery E; Blanluet M; El-Hayek S; Stoppa-Lyonnet D; Megarbane A
    J Pediatr Hematol Oncol; 2021 Jul; 43(5):e727-e735. PubMed ID: 32947577
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.