Optimal First-Line Treatment of Chronic Myeloid Leukemia: How to Use Imatinib and What Role for Newer Drugs?
- Published in:
- Oncology (08909091), 2007, v. 21, n. 6, p. 653
- By:
- Publication type:
- Article
Works matching DE "HUMAN cytogenetics"
Results: 690
1
2
Evolving Classification and Management of Myeloplastic Syndrome.
- Published in:
- Oncology (08909091), 2007, v. 21, n. 1, p. 57
- By:
- Publication type:
- Article
3
Embryoscopy and karyotype findings of repeated miscarriages in recurrent pregnancy loss and spontaneous pregnancy loss.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 8, p. 1401, doi. 10.1007/s10815-018-1226-1
- By:
- Publication type:
- Article
4
Ultrastructural and cytogenetic analyses of mature human oocyte dysmorphisms with respect to clinical outcomes.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2016, v. 33, n. 8, p. 1041, doi. 10.1007/s10815-016-0739-8
- By:
- Publication type:
- Article
5
Molecular analysis of products of conception obtained by hysteroembryoscopy from infertile couples.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2015, v. 32, n. 5, p. 839, doi. 10.1007/s10815-015-0460-z
- By:
- Publication type:
- Article
6
Karyotype analysis in large-sample infertile couples living in Central China: a study of 14965 couples.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 4, p. 547, doi. 10.1007/s10815-013-9964-6
- By:
- Publication type:
- Article
7
Chromosomal integrity of human preimplantation embryos at different days post fertilization.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 5, p. 633, doi. 10.1007/s10815-013-9988-y
- By:
- Publication type:
- Article
8
Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 11, p. 1091, doi. 10.1007/s10815-011-9633-6
- By:
- Publication type:
- Article
9
Broadening our understanding by the use of molecular cytogenetic techniques: full monosomy 21.
- Published in:
- 2011
- By:
- Publication type:
- Report
10
Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in Southern region of India: report and review.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 2, p. 145, doi. 10.1007/s10815-010-9492-6
- By:
- Publication type:
- Article
11
Cytogenetic abnormalities detected in patients with non-obstructive azoospermia and severe oligozoospermia.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2010, v. 27, n. 1, p. 17, doi. 10.1007/s10815-009-9366-y
- By:
- Publication type:
- Article
12
Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2009, v. 26, n. 2/3, p. 119, doi. 10.1007/s10815-009-9296-8
- By:
- Publication type:
- Article
13
Cytogenetic testing of anembryonic pregnancies compared to embryonic missed abortions.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2007, v. 24, n. 11, p. 521, doi. 10.1007/s10815-007-9166-1
- By:
- Publication type:
- Article
14
Chemically induced premature chromosome condensation in short-term cultured human peripheral lymphocytes: applications to biodosimetry.
- Published in:
- Biotechnic & Histochemistry, 2007, v. 82, n. 1, p. 29, doi. 10.1080/10520290701257153
- By:
- Publication type:
- Article
15
Chromosomal evolution of Arvicolinae (Cricetidae, Rodentia). I. The genome homology of tundra vole, field vole, mouse and golden hamster revealed by comparative chromosome painting.
- Published in:
- Chromosome Research, 2007, v. 15, n. 4, p. 447, doi. 10.1007/s10577-007-1137-y
- By:
- Publication type:
- Article
16
In vitro effect of fenthion on human lymphocytes.
- Published in:
- Bulletin of Environmental Contamination & Toxicology, 1991, v. 47, n. 2, p. 316, doi. 10.1007/BF01688658
- By:
- Publication type:
- Article
17
T cell development: Lead role for BCL-6 in T<sub>FH</sub> cell development.
- Published in:
- Nature Reviews Immunology, 2009, v. 9, n. 9, p. 605, doi. 10.1038/nri2626
- By:
- Publication type:
- Article
18
187. ANALYSIS OF CHROMOSOMAL ABERRATIONS AND SCE'S IN OCCUPATIONALLY LEAD EXPOSED POPULATION.
- Published in:
- 2002
- Publication type:
- Abstract
19
INFLUENCE OF MERCURY VAPORS ON LYMPHOCYTES IN VIVO AND ON THEIR SUSCEPTIBILITY TO UV-C AND X-RAYS, AND REPAIR EFFICIENCY IN VITRO.
- Published in:
- Medycyna Pracy, 2005, v. 56, n. 4, p. 303
- By:
- Publication type:
- Article
20
KARYOTYPE DISORDERS AMONG MEN AND WOMEN DIAGNOSED WITH INFERTILITY.
- Published in:
- Bulletin of Taras Shevchenko National University of Kyiv / Vestnik Kievskogo Nacional'Nogo Universiteta Imeni Tarasa Ševčenko, 2013, v. 64, n. 2, p. 38
- By:
- Publication type:
- Article
21
Coexistence of p210<sup>BCR-ABL</sup> and CBFβ-MYH11 fusion genes in myeloid leukemia: A report of 4 cases.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
22
Clinical characteristics and laboratory analyses of acute myeloid leukemia with t(16;21)(p11;q22).
- Published in:
- Oncology Letters, 2015, v. 9, n. 5, p. 2244, doi. 10.3892/ol.2015.3051
- By:
- Publication type:
- Article
23
Prognostic value of molecular markers and cytogenetic alterations that characterize breast cancer precursor lesions (Review).
- Published in:
- Oncology Letters, 2013, v. 6, n. 5, p. 1181, doi. 10.3892/ol.2013.1589
- By:
- Publication type:
- Article
24
Variations in the Phagosomal Environment of Human Neutrophils and Mononuclear Phagocyte Subsets.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00188
- By:
- Publication type:
- Article
25
Fragile-X syndrome in North East Essex: towards systematic screening: clinical selection.
- Published in:
- Journal of Intellectual Disability Research, 1994, v. 38, n. 1, p. 27, doi. 10.1111/j.1365-2788.1994.tb00344.x
- By:
- Publication type:
- Article
26
Chromosome fragility in the Lennox-Gastaut epilepsy syndrome.
- Published in:
- Journal of Intellectual Disability Research, 1992, v. 36, n. 5, p. 435, doi. 10.1111/j.1365-2788.1992.tb00561.x
- By:
- Publication type:
- Article
27
The protein expression profile of meningioma cells is associated with distinct cytogenetic tumour subgroups.
- Published in:
- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 3, p. 319, doi. 10.1111/nan.12127
- By:
- Publication type:
- Article
28
Specific abnormalities versus number of abnormalities and cytogenetic scoring systems for outcome prediction after allogeneic hematopoietic SCT for myelodysplastic syndromes.
- Published in:
- Bone Marrow Transplantation, 2014, v. 49, n. 8, p. 1022, doi. 10.1038/bmt.2014.87
- By:
- Publication type:
- Article
29
Duration of first remission, hematopoietic cell transplantation-specific comorbidity index and patient age predict survival of patients with AML transplanted in second CR.
- Published in:
- Bone Marrow Transplantation, 2013, v. 48, n. 11, p. 1450, doi. 10.1038/bmt.2013.71
- By:
- Publication type:
- Article
30
Induction of graft versus malignancy effect after unrelated allogeneic PBSCT using donor lymphocyte infusions derived from frozen aliquots of the original graft.
- Published in:
- Bone Marrow Transplantation, 2012, v. 47, n. 2, p. 277, doi. 10.1038/bmt.2011.45
- By:
- Publication type:
- Article
31
Congenital acute lymphoblastic leukemia: a two-case report and a review of the literature.
- Published in:
- 2011
- By:
- Publication type:
- journal article
32
Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism.
- Published in:
- 2010
- By:
- Publication type:
- journal article
33
Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?
- Published in:
- 2004
- By:
- Publication type:
- journal article
34
Transient Myelodysplastic Syndrome Associated with Isochromosome 7q Abnormality.
- Published in:
- Pediatric Hematology & Oncology, 2003, v. 20, n. 7, p. 539, doi. 10.1080/08880010390232754
- By:
- Publication type:
- Article
35
Linfoma no Hodgkin y leucemia mieloide crónica metacrónica en una paciente. Reporte de un caso.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
36
Chronic lymphocytic leukemia-associated chromosomal abnormalities and miRNA deregulation.
- Published in:
- Application of Clinical Genetics, 2012, v. 5, p. 21, doi. 10.2147/TACG.S18669
- By:
- Publication type:
- Article
37
Array CGH as a first-tier test for neonates with congenital heart disease.
- Published in:
- 2015
- By:
- Publication type:
- journal article
38
Differentiation between malignant melanomas and benign melanocytic nevi by computerized DNA cytometry of imprint specimens.
- Published in:
- Journal of Cutaneous Pathology, 1994, v. 21, n. 1, p. 7, doi. 10.1111/j.1600-0560.1994.tb00684.x
- By:
- Publication type:
- Article
39
Interphase cytogenetics of melanocytic neoplasms: numerical aberrations of chromosomes can be detected in interphase nuclei using centromeric DNA probes.
- Published in:
- Journal of Cutaneous Pathology, 1994, v. 21, n. 1, p. 1, doi. 10.1111/j.1600-0560.1994.tb00683.x
- By:
- Publication type:
- Article
40
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 12, p. 1592, doi. 10.1038/ejhg.2009.90
- By:
- Publication type:
- Article
41
4q32–q35 and 6q16–q22 are valuable candidate regions for split hand/foot malformation.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 8, p. 1086, doi. 10.1038/ejhg.2009.11
- By:
- Publication type:
- Article
42
Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 6, p. 696, doi. 10.1038/ejhg.2008.7
- By:
- Publication type:
- Article
43
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf–Hirschhorn syndrome.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1132, doi. 10.1038/sj.ejhg.5201899
- By:
- Publication type:
- Article
44
How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 917, doi. 10.1038/sj.ejhg.5201867
- By:
- Publication type:
- Article
45
A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 8, p. 971, doi. 10.1038/sj.ejhg.5201635
- By:
- Publication type:
- Article
46
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 11, p. 1192, doi. 10.1038/sj.ejhg.5201473
- By:
- Publication type:
- Article
47
Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 1, p. 6, doi. 10.1038/sj.ejhg.5201279
- By:
- Publication type:
- Article
48
Clinical experience with multiplex ligation-dependent probe amplification for microdeletion syndromes in prenatal diagnosis: 7522 pregnant Korean women.
- Published in:
- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0422-8
- By:
- Publication type:
- Article
49
Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.
- Published in:
- Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0395-z
- By:
- Publication type:
- Article
50
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44).
- Published in:
- 2018
- By:
- Publication type:
- Case Study