A 20-year perspective on the International Fanconi Anemia Registry (IFAR).
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Marianne Berwick | J. Satagopan | P. Giampietro | Bhuvanesh Singh | S. Batish | D. Kutler | M. Berwick | A. Auerbach | H. Hanenberg | David I Kutler | Jaya Satagopan | Bhuvanesh Singh | Helmut Hanenberg | Arleen D Auerbach | Sat Dev Batish | Philip F Giampietro
[1] Hans Joenje,et al. The emerging genetic and molecular basis of Fanconi anaemia , 2001, Nature Reviews Genetics.
[2] Hans Joenje,et al. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA , 1996, Nature Genetics.
[3] C. Mathew,et al. Positional cloning of the Fanconi anaemia group A gene , 1996, Nature Genetics.
[4] C. Mathew,et al. Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A. , 2000, American journal of human genetics.
[5] J. Greenbaum,et al. Spectrum of sequence variation in the FANCG gene: An International Fanconi Anemia Registry (IFAR) study , 2003, Human mutation.
[6] S. Batish,et al. Evaluation of Growth and Hormonal Status in Patients Referred to the International Fanconi Anemia Registry , 2001, Pediatrics.
[7] S. Ganesan,et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. , 2001, Molecular cell.
[8] H. Olsson. Cancer risks in BRCA2 mutation carriers. , 1999, Journal of the National Cancer Institute.
[9] S. Batish,et al. Spectrum of sequence variations in the FANCA gene: An International Fanconi Anemia Registry (IFAR) study , 2003, Human mutation.
[10] A. Rogatko,et al. International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity. , 1989, Blood.
[11] W. R. Hart,et al. Multiple squamous‐cell carcinomas in fanconi's anemia , 1982, Cancer.
[12] R. G. Allen,et al. Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry. , 1991, Cancer genetics and cytogenetics.
[13] Bo Xu,et al. Convergence of the Fanconi Anemia and Ataxia Telangiectasia Signaling Pathways , 2002, Cell.
[14] E L Kaplan. NON-PARAMETRIC ESTIMATION FROM INCOMPLETE OBSERVATION , 1958 .
[15] Q. Waisfisz,et al. The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG. , 2000, Human molecular genetics.
[16] M. Swift,et al. Reassessment of cancer predisposition of Fanconi anemia heterozygotes. , 1980, Journal of the National Cancer Institute.
[17] A D Auerbach,et al. Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study. , 1997, Blood.
[18] W. R. Shannon,et al. Cloning of cDNAs for Fanconi's anaemia by functional complementation , 1992, Nature.
[19] D. Näf,et al. The Fanconi anaemia proteins, FAA and FAC interact to form a nuclear complex , 1997, Nature Genetics.
[20] N. Dracopoli,et al. Current protocols in human genetics , 1994 .
[21] R. Gale,et al. Hematologic Abnormalities in Fanconi Anemia: An International Fanconi Anemia Registry Study , 1994 .
[22] C G Mathew,et al. Isolation of a cDNA representing the Fanconi anemia complementation group E gene. , 2000, American journal of human genetics.
[23] A. D’Andrea,et al. The fanconi anemia proteins FANCA and FANCG stabilize each other and promote the nuclear accumulation of the Fanconi anemia complex. , 2000, Blood.
[24] B. Alter,et al. Fanconi anemia: myelodysplasia as a predictor of outcome. , 2000, Cancer genetics and cytogenetics.
[25] B. Alter. Fanconi's anemia and malignancies , 1996, American journal of hematology.
[26] Hans Joenje,et al. The Fanconi anaemia group G gene FANCG is identical with XRCC9 , 1998, Nature Genetics.
[27] J. Shah,et al. High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. , 2003, Archives of otolaryngology--head & neck surgery.
[28] P. Giampietro,et al. The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry. , 1993, Pediatrics.
[29] P. Giampietro,et al. Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry Study. , 1997, American journal of medical genetics.
[30] F. Oski,et al. Hematology of Infancy and Childhood , 1974 .
[31] G. Draper,et al. Incidence of second primary tumours among childhood cancer survivors. , 1987, British Journal of Cancer.
[32] C. Mathew,et al. Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3 , 1999, British Journal of Cancer.
[33] David A. Williams,et al. Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool. , 2002, Experimental hematology.
[34] Hans Joenje,et al. The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM , 2000, Nature Genetics.
[35] M. Buchwald,et al. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9 , 1992, Nature Genetics.
[36] K. Kinzler,et al. The Genetic Basis of Human Cancer , 1997 .
[37] A. D’Andrea,et al. Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells. , 2001, Experimental hematology.
[38] R. Gray. A Class of $K$-Sample Tests for Comparing the Cumulative Incidence of a Competing Risk , 1988 .
[39] R. Moses,et al. Positional cloning of a novel Fanconi anemia gene, FANCD2. , 2001, Molecular cell.
[40] Hans Joenje,et al. Biallelic Inactivation of BRCA2 in Fanconi Anemia , 2002, Science.
[41] H. Deeg,et al. Malignancies after marrow transplantation for aplastic anemia and fanconi anemia: a joint Seattle and Paris analysis of results in 700 patients. , 1996, Blood.
[42] B. Alter. Bone marrow failure syndromes. , 1991, Clinics in laboratory medicine.
[43] A. Auerbach,et al. Carrier frequency of the IVS4 + 4 A-->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population. , 1995, Blood.
[44] A. Neder,et al. Head and neck carcinoma in Fanconi's anaemia--report of a case and review of the literature. , 1995, European journal of cancer. Part B, Oral oncology.