WordNet

chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number

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1. 自然早産のリスクを低下させるためのプロゲステロン補充 progesterone supplementation to reduce the risk of spontaneous preterm birth
2. 急性骨髄性白血病の分類 classification of acute myeloid leukemia
3. 急性骨髄性白血病における細胞遺伝学 cytogenetics in acute myeloid leukemia
4. 形質細胞白血病 plasma cell leukemia
5. 急性骨髄性白血病の予後 prognosis of acute myeloid leukemia

Medulloblastoma, WNT-activated/SHH-activated: clinical impact of molecular analysis and histogenetic evaluation.

Cambruzzi E1,2,3,4,5.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery.Childs Nerv Syst.2018 May;34(5):809-815. doi: 10.1007/s00381-018-3765-2. Epub 2018 Mar 26.
PMID 29582169

"Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain.

Chapiro E1,2,3, Lesty C2,3, Gabillaud C3, Durot E4, Bouzy S3, Armand M1,2,3, Le Garff-Tavernier M1,3, Bougacha N1,2, Struski S5, Bidet A6, Laharanne E6, Barin C7, Veronese L8, Prié N8, Eclache V9, Gaillard B10, Michaux L11, Lefebvre C12, Gaillard JB13, Terré C14, Penther D15, Bastard C15, Nadal N16, Fert-Ferrer S17, Auger N18, Godon C19, Sutton L20, Tournilhac O21, Susin SA1,2, Nguyen-Khac F1,2,3; GroupeFrancophone de Cytogénétique Hématologique(GFCH) and the French Innovative Leukemia Organization (FILO) group.
American journal of hematology.Am J Hematol.2018 Mar;93(3):375-382. doi: 10.1002/ajh.24990. Epub 2017 Dec 18.
PMID 29194741

TP53 Mutation and Its Prognostic Significance in Waldenstrom's Macroglobulinemia.

Poulain S1,2,3, Roumier C2,3, Bertrand E3, Renneville A2,3, Caillault-Venet A2, Doye E2, Geffroy S3, Sebda S2, Nibourel O2,3, Nudel M4, Herbaux C4, Renaud L2, Tomowiak C5,6, Guidez S5,6, Tricot S1, Roche-Lestienne C2,3, Quesnel B3,4, Preudhomme C2,3, Leleu X7,6.
Clinical cancer research : an official journal of the American Association for Cancer Research.Clin Cancer Res.2017 Oct 15;23(20):6325-6335. doi: 10.1158/1078-0432.CCR-17-0007. Epub 2017 Jul 28.
PMID 28754818

Analysis of genomic alterations on urological malignancies by fluorescence in situ hybridization