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Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France.
- Published in:
- Diabetologia, 2002, v. 45, n. 3, p. 454, doi. 10.1007/s00125-001-0741-1
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- Article
Community Care Networks: Linking Vision to Outcomes for Community Health Improvement.
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- Medical Care Research & Review, 2003, v. 60, n. 4, p. 95S, doi. 10.1177/1077558703259096
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- Publication type:
- Article
Prenatal diagnosis of trisomy 21 by i(21q): a rare case of fetoplacental chromosomal discrepancy.
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- Prenatal Diagnosis, 2002, v. 22, n. 10, p. 856, doi. 10.1002/pd.425
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- Article
Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communication.
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- Diabetic Medicine, 2015, v. 32, n. 5, p. 701, doi. 10.1111/dme.12670
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- Article
CORRESPONDENCE.
- Published in:
- Leukemia (08876924), 2002, v. 16, n. 4, p. 762
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- Article
Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia.
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- 2001
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- Publication type:
- journal article
Long-term results of three randomized trials (58831, 58832, 58881) in childhood acute lymphoblastic leukemia: a CLCG-EORTC report. Children Leukemia Cooperative Group.
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- 2000
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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.
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- 1999
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- journal article
High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia.
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- 1998
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- Publication type:
- journal article
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia.
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- 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
Pharmacogenetics of CYP3A5 and effects of corticosteroids in children treated for acute lymphoblastic leukemia.
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- Clinical Pharmacology & Therapeutics, 2004, v. 75, n. 2, p. P20, doi. 10.1016/j.clpt.2003.11.075
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- Article
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q<sub>10</sub> deficiency.
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- Journal of Inherited Metabolic Disease, 2007, v. 30, n. 5, p. 827, doi. 10.1007/s10545-007-0612-0
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- Article
Refinement of IKZF1 status in pediatric Philadelphia-positive acute lymphoblastic leukemia.
- Published in:
- 2015
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- Publication type:
- Letter
In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia.
- Published in:
- Leukemia (08876924), 2013, v. 27, n. 12, p. 2404, doi. 10.1038/leu.2013.203
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- Publication type:
- Article
The MLL recombinome of acute leukemias in 2013.
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- Leukemia (08876924), 2013, v. 27, n. 11, p. 2165, doi. 10.1038/leu.2013.135
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- Publication type:
- Article
Flow cytometry and IG/TCR quantitative PCR for minimal residual disease quantitation in acute lymphoblastic leukemia: a French multicenter prospective study on behalf of the FRALLE, EORTC and GRAALL.
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- Leukemia (08876924), 2013, v. 27, n. 2, p. 370, doi. 10.1038/leu.2012.234
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- Article
The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantation.
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- Leukemia (08876924), 2012, v. 26, n. 8, p. 1821, doi. 10.1038/leu.2012.66
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- Publication type:
- Article
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
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- Leukemia (08876924), 2012, v. 26, n. 5, p. 902, doi. 10.1038/leu.2011.302
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- Publication type:
- Article
A new recurrent translocation t(11;14)(q24;q32) involving IGH@ and miR-125b-1 in B-cell progenitor acute lymphoblastic leukemia.
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- Leukemia (08876924), 2010, v. 24, n. 7, p. 1362, doi. 10.1038/leu.2010.93
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- Article
Activating mutation in the TSLPR gene in B-cell precursor lymphoblastic leukemia.
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- Leukemia (08876924), 2010, v. 24, n. 3, p. 642, doi. 10.1038/leu.2009.231
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- Article
Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18–20 September 2008.
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- Leukemia (08876924), 2010, v. 24, n. 3, p. 521, doi. 10.1038/leu.2009.268
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- Publication type:
- Article
Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.
- Published in:
- 2010
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- Publication type:
- Letter
PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study.
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- 2009
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- Publication type:
- journal article
New insights to the MLL recombinome of acute leukemias.
- Published in:
- 2009
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- Publication type:
- journal article
Childhood secondary ALL after ALL treatment.
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- Leukemia (08876924), 2007, v. 21, n. 7, p. 1431, doi. 10.1038/sj.leu.2404718
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- Publication type:
- Article
Analysis of minimal residual disease by Ig/TCR gene rearrangements: guidelines for interpretation of real-time quantitative PCR data.
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- Leukemia (08876924), 2007, v. 21, n. 4, p. 604, doi. 10.1038/sj.leu.2404586
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- Publication type:
- Article
Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRβ-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique Hématologique.
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- Leukemia (08876924), 2007, v. 21, n. 1, p. 121, doi. 10.1038/sj.leu.2404410
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- Publication type:
- Article
Standardization and quality control studies of ‘real-time’ quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - A Europe Against Cancer Program.
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- Leukemia (08876924), 2003, v. 17, n. 12, p. 2318, doi. 10.1038/sj.leu.2403135
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- Article
Quantitative analysis of chimerism after allogeneic stem cell transplantation by PCR amplification of microsatellite markers and capillary electrophoresis with fluorescence detection: the Paris–Robert Debré experience.
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- Leukemia (08876924), 2003, v. 17, n. 1, p. 241, doi. 10.1038/sj.leu.2402762
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- Publication type:
- Article
Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma.
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- British Journal of Cancer, 2004, v. 90, n. 2, p. 503, doi. 10.1038/sj.bjc.6601503
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- Article
'Cobblestone' papillomatous linear papules of the upper lip: a new sign of Costello syndrome.
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- British Journal of Dermatology, 2013, v. 168, n. 4, p. 903, doi. 10.1111/bjd.12103
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- Article