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CORRESPONDENCE.
- Published in:
- Leukemia (08876924), 2002, v. 16, n. 4, p. 762
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- Publication type:
- Article
Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia.
- Published in:
- 2001
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- Publication type:
- journal article
Mapping of chromosome 20 for loss of heterozygosity in childhood ALL reveals a 1,000-kb deletion in one patient.
- Published in:
- 1999
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- Publication type:
- journal article
High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia.
- Published in:
- 1998
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- Publication type:
- journal article
Study of the thrombopoitin receptor in essential thrombocythemia.
- Published in:
- 1997
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- Publication type:
- journal article
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia.
- Published in:
- 1997
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- Publication type:
- journal article
Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm.
- Published in:
- 1997
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- Publication type:
- journal article
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemia.
- Published in:
- Cytogenetic & Genome Research, 1999, v. 85, n. 3/4, p. 260, doi. 10.1159/000015308
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- Publication type:
- Article
Detection and identification of mycobacteria by amplification of mycobacterial DNA.
- Published in:
- Molecular Microbiology, 1989, v. 3, n. 7, p. 843, doi. 10.1111/j.1365-2958.1989.tb00233.x
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- Publication type:
- Article
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemia.
- Published in:
- Cytogenetics & Cell Genetics, 1999, v. 85, n. 3/4, p. 260, doi. 10.1159/000015308
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- Publication type:
- Article
Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assay.
- Published in:
- 2012
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- Publication type:
- Journal Article
Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study.
- Published in:
- 2006
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- Publication type:
- Journal Article
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases.
- Published in:
- European Journal of Clinical Investigation, 2001, v. 31, n. 5, p. 382, doi. 10.1046/j.1365-2362.2001.00829.x
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- Publication type:
- Article
Essential thrombocythemias without V617F JAK2 mutation are clonal hematopoietic stem cell disorders.
- Published in:
- 2006
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- Publication type:
- Letter
Identification of a new mutation responsible for hepatoerythropoietic porphyria.
- Published in:
- European Journal of Clinical Investigation, 1991, v. 21, n. 2, p. 225, doi. 10.1111/j.1365-2362.1991.tb01814.x
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- Publication type:
- Article
Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminase.
- Published in:
- European Journal of Clinical Investigation, 1989, v. 19, n. 5, p. 415, doi. 10.1111/j.1365-2362.1989.tb00252.x
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- Publication type:
- Article
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.
- Published in:
- 2006
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- Publication type:
- journal article
Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma.
- Published in:
- British Journal of Cancer, 2004, v. 90, n. 2, p. 503, doi. 10.1038/sj.bjc.6601503
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- Publication type:
- Article
Comment on: Park et al. Association of serum ferritin and the development of metabolic syndrome in middle-aged Korean men: a 5-year follow-up study. Diabetes Care 2012;35:2521-2526.
- Published in:
- 2012
- By:
- Publication type:
- Letter
Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in a general population: Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR)
- Published in:
- 2007
- By:
- Publication type:
- Journal Article
Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extension.
- Published in:
- Human Mutation, 2000, v. 16, n. 3, p. 253, doi. 10.1002/1098-1004(200009)16:3<253::AID-HUMU8>3.0.CO;2-8
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- Publication type:
- Article
Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(−) hereditary elliptocytosis.
- Published in:
- Human Mutation, 1995, v. 5, n. 4, p. 339, doi. 10.1002/humu.1380050412
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- Publication type:
- Article
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C.
- Published in:
- British Journal of Dermatology, 2013, v. 168, n. 5, p. 1109, doi. 10.1111/bjd.12183
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- Publication type:
- Article
Interactions between ultraviolet light exposure and DNA repair gene polymorphisms may increase melanoma risk.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survival.
- Published in:
- British Journal of Dermatology, 2008, v. 159, n. 4, p. 968, doi. 10.1111/j.1365-2133.2008.08791.x
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- Publication type:
- Article
EDNRB gene variants and melanoma risk in two southern European populations.
- Published in:
- Clinical & Experimental Dermatology, 2011, v. 36, n. 7, p. 782, doi. 10.1111/j.1365-2230.2011.04062.x
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- Publication type:
- Article
Duodenal expression of NF-E2 in mouse models of altered iron metabolism.
- Published in:
- British Journal of Haematology, 1995, v. 91, n. 2, p. 483, doi. 10.1111/j.1365-2141.1995.tb05328.x
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- Publication type:
- Article