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- 约1.96千字
- 约 96页
- 2021-05-24 发布于江苏
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Clinical Application of
Cancer Cytogenomics;细胞基因组( Cytogenomics );细胞基因组、细胞基因组标志;;;Agilent G2565AA Microarray Scanner System at
MDACC;细胞基因组疾病;非肿瘤细胞基因组疾病;Contiguous gene syndrome/
microdeletion syndrome;;智力低下 /aCGH
-Who need the test?
? Individuals with unexplained
developmental/intellectual delay;Agilent: 580 Kb deletion 2p22.3;;FISH with a
red-labeled;;Acute Leukemia in DS;Acute leukemia in Down syndrome; 细胞基因组标志在肿瘤的诊断、
预后、随访跟踪、治疗上的临床应用
? 血液肿瘤
? 淋巴瘤
? 骨髓瘤
? 白血病;? 诊断;;t(8;14) karyotype;;;t(9;22)(q34;q11.2) - CML;Cryptic t(9;22);Interferon a
Gleevec;;Subtype;- 急性淋巴细胞白血病
acute lymphoblastic leukemia;Pediatric ALL;Diagnosis;;Tumors;Probes;SYT/18q11.2 positive in Synovial Sarcoma;Probes;SYT/18q11.2/ Synovial Sarcoma;肿瘤细胞基因组学;预后; 肿瘤预后应用
? ASS loss in t(9;22) positive CML associated with resistance
to interferon therapy;Trisomy 11 as the sole abnormality in
MDS;CLL FISH panel;AML1 Amplification in AML;MLL Amplification;T(4;14)(p16;q32) in myeloma;ASS deletion in CML;图片录用于江西省妇幼保健院 李隆玉教授;;治 疗 ( THEAPEUTICS );酒窝征 (A) ,橘皮征( B) ,炎性乳腺癌( C) ,湿疹样癌 ( D);Her2 amp/Herceptin;PDGFRA rea/Greevec;ALK, ROS1, RET rea in lung cancer;C-MET amp/ARQ197, MP470;新研发;Cancer Cytogenomic;ELL (eleven nineteen lysin rich
leukemia gene);MLL;Comparison;B-ALL with t(14;19)(q32;p13.1);Pt;It is a challenge to identify the subtle;;Home-brew FISH EPOR probe;Labeling the FISH Probes;Clinical Features;After IGH confirmation, Where is partner to
match?
t(1;19)(q23;p13.3)
t(11;19)(q23;p13.3)
E2A
ENL*;? Male
? 6 months old
? Dx with ALL
? B-cell markers
including CD10+,
CD19+
? BMT
? Survival 6 mons;Plasma Cell Myeloma;;;;;;;遗传咨询;Clinical Integrated;Genomic Analysis by Array Comparative Genomic Hybridization of Primary Myelofibrosis with Isolated del(13q)
Gary Lu, 1 Keyur P. Patel, 1 Roberto N. Miranda, 1 L Jeffrey Medeiros, 1 Tianjian Chen, 2 Bal Mukund Mishra, 1 Ronald Abraham, 1
Ramya Muddasani, 1 Meenakshi Mehrotra, 1 and Raja Luthra 1;
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