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Academic Journal

Tri-ing to decipher trisomy AML.

  • Authors : Shimony S; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.; Rabin Medical Center and Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Subjects: Trisomy* ; Leukemia, Myeloid, Acute*; Humans

  • Source: British journal of haematology [Br J Haematol] 2024 Mar; Vol. 204 (3), pp. 751-752. Date of Electronic Publication: 2024 Jan 08.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Prognostic impact of trisomy 21 in follicular lymphoma.

  • Authors : Mitsui T; Department of Haematology, Gunma University Graduate School of Medicine, Maebashi, Japan.; Yokohama A

Subjects: Trisomy*; Chromosomes, Human, Pair 21/Chromosomes, Human, Pair 21/Chromosomes, Human, Pair 21/*genetics ; Lymphoma, Follicular/Lymphoma, Follicular/Lymphoma, Follicular/*genetics

  • Source: British journal of haematology [Br J Haematol] 2019 Feb; Vol. 184 (4), pp. 570-577. Date of Electronic Publication: 2018 Nov 12.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies.

  • Authors : Drevon L; Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris (APHP), University Paris Diderot (Paris 7), Paris, France.; Marceau A

Subjects: Myelodysplastic Syndromes/Myelodysplastic Syndromes/Myelodysplastic Syndromes/*genetics ; Myeloproliferative Disorders/Myeloproliferative Disorders/Myeloproliferative Disorders/*genetics ; Trisomy/Trisomy/Trisomy/*geneticsChromosome 8, trisomy

  • Source: British journal of haematology [Br J Haematol] 2018 Sep; Vol. 182 (6), pp. 843-850. Date of Electronic Publication: 2018 Jul 13.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Report

A special type of chromosome 1 abnormality in myelodysplastic syndrome patients: duplication 1q.

  • Authors : Yu Y; Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases, the First Affiliated Hospital of Soochow University, Suzhou, P.R. China.; Collaborative Innovation Center of Hematology, Soochow University, Suzhou, P.R. China.

Subjects: Chromosome Aberrations* ; Trisomy*; Chromosomes, Human, Pair 1/Chromosomes, Human, Pair 1/Chromosomes, Human, Pair 1/*ultrastructure

  • Source: British journal of haematology [Br J Haematol] 2020 Jun; Vol. 189 (5), pp. e218-e221. Date of Electronic Publication: 2020 Apr 16.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes.

  • Authors : Saumell S; Laboratori de Citologia Hematològica, Laboratori de Citogenètica Molecular, Serveis de Patologia i d'Hematologia Cl\xEDnica, Hospital del Mar, Barcelona, Spain.; Florensa L

Subjects: Chromosome Aberrations* ; Trisomy*; Myelodysplastic Syndromes/Myelodysplastic Syndromes/Myelodysplastic Syndromes/*genetics Chromosome 8, trisomy

  • Source: British journal of haematology [Br J Haematol] 2012 Nov; Vol. 159 (3), pp. 311-21. Date of Electronic Publication: 2012 Sep 07.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.

  • Authors : Ripperger T; Institute of Cell and Molecular Pathology, Hannover Medical School, Hannover, Germany.; Tauscher M

Subjects: Chromosomes, Human, Pair 8*/Chromosomes, Human, Pair 8*/Chromosomes, Human, Pair 8*/genetics ; Mosaicism* ; Trisomy*Chromosome 7, monosomy

  • Source: British journal of haematology [Br J Haematol] 2011 Oct; Vol. 155 (2), pp. 209-17. Date of Electronic Publication: 2011 Aug 18.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Editorial & Opinion

Trisomy 12 is associated with an abbreviated redistribution lymphocytosis during treatment with the BTK inhibitor ibrutinib in patients with chronic lymphocytic leukaemia.

  • Authors : Thompson PA; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. .; Ferrajoli A

Subjects: Leukemia, Lymphocytic, Chronic, B-Cell/Leukemia, Lymphocytic, Chronic, B-Cell/Leukemia, Lymphocytic, Chronic, B-Cell/*drug therapy ; Leukemia, Lymphocytic, Chronic, B-Cell/Leukemia, Lymphocytic, Chronic, B-Cell/Leukemia, Lymphocytic, Chronic, B-Cell/*genetics ; Lymphocytosis/Lymphocytosis/Lymphocytosis/*genetics Chromosome 12, 12p trisomy

  • Source: British journal of haematology [Br J Haematol] 2015 Jul; Vol. 170 (1), pp. 125-8. Date of Electronic Publication: 2014 Dec 18.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliferative disorder.

  • Authors : Carpenter E; Department of Haematology and MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Oxford Radcliffe Hospital, Oxford OX3 9DU, UK.; Valverde-Garduno V

Subjects: Mutation* ; Trisomy*; Chromosomes, Human, Pair 21/Chromosomes, Human, Pair 21/Chromosomes, Human, Pair 21/*genetics

  • Source: British journal of haematology [Br J Haematol] 2005 Feb; Vol. 128 (4), pp. 548-51.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print Cited Medium: Print ISSN: 0007-1048 (Print)

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Academic Journal

The incidences of trisomy 8, trisomy 9 and D20S108 deletion in polycythaemia vera: an analysis of blood granulocytes using interphase fluorescence in situ hybridization.

  • Authors : Westwood NB; Department of Haematological Medicine, Guy's, King's & St Thomas' Medical School, King's College London, UK. ; Gruszka-Westwood AM

Subjects: Chromosomes, Human, Pair 8* ; Chromosomes, Human, Pair 9* ; Gene Deletion*

  • Source: British journal of haematology [Br J Haematol] 2000 Sep; Vol. 110 (4), pp. 839-46.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print Cited Medium: Print ISSN: 0007-1048 (Print)

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Academic Journal

Trisomy 3 in two paediatric post-transplant lymphomas.

  • Authors : Gallego MS; Cytogenetics Laboratory, Department of Genetics, Prof. Dr. Juan B. Garrahan Pediatric Hospital, Combate de los Pozos 1881, Buenos Aires C.P 1245, Argentina. ; Bernasconi A

Subjects: Chromosomes, Human, Pair 3* ; Kidney Transplantation* ; Liver Transplantation*

  • Source: British journal of haematology [Br J Haematol] 2002 Jun; Vol. 117 (3), pp. 558-62.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print Cited Medium: Print ISSN: 0007-1048 (Print)

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  • 1-10 of  1,604 results for ""Trisomy""