182 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
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GSE243055
A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias [Copy number analysis]
  • Link icon Homo sapiens
4 Cristina Mecucci Apr 30, 2024
GSE243056
A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias
  • Link icon Homo sapiens
19 Cristina Mecucci Apr 30, 2024
GSE243782
K-562 cell lines
  • Link icon Homo sapiens
3 Fumio Kasai Jan 01, 2024
GSE240546
Comparison of CNV in 6 ostosarcoma cell lines
  • Link icon Homo sapiens
6 Chia-Ho Cheng Nov 22, 2023
GSE230532
Prenatal Diagnosis and Clinical Analysis of Talipes Equinovarus by Chromosomal Microarray Analysis
  • Link icon Homo sapiens
131 Xiaorui Xie Oct 22, 2023
GSE197838
Affymetrix SNP array data for acute lymphoblastic leukemia samples
  • Link icon Homo sapiens
56 Mayur Parihar Sep 30, 2023
GSE235430
Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele: a single tertiary center experience
  • Link icon Homo sapiens
5 Yanting Que Sep 27, 2023
GSE240611
Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications
  • Link icon Homo sapiens
26 Hongguo Zhang Aug 14, 2023
GSE178421
Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma [Cytoscan]
  • Link icon Homo sapiens
23 Joan Enric Ramiz-Zaldivar Jun 05, 2023
GSE178427
Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma
  • Link icon Homo sapiens
35 Joan Enric Ramiz-Zaldivar Jun 05, 2023
GSE233748
Affymetrix SNP array data for an INAD patient
  • Link icon Homo sapiens
1 yongxue lv May 31, 2023
GSE207887
Chromosomal abnormalities of 564 miscarriages
  • Link icon Homo sapiens
564 Haiwei Wang May 21, 2023
GSE230763
Can non-invasive prenatal screening based on cell-free fetal DNA be utilized to assess chromosome abnormalities in fetuses with increased Nuchal Translucency?
  • Link icon Homo sapiens
129 su linjuan Apr 30, 2023
GSE213813
Affymetrix SNP array data for induced pluripotent stem cell line
  • Link icon Homo sapiens
4 Yolanda Aguilera Feb 15, 2023
GSE223242
Genetic analysis, ultrasound phenotype, and pregnancy outcome of fetuses with Xp22.33 or Yp11.32 microdeletion
  • Link icon Homo sapiens
5 Hailong Huang Jan 24, 2023
GSE216574
Double-deletion of 1p32 defines ultra-high-risk myeloma, but monoallelic del(1p32) remains a strong prognostic factor
  • Link icon Homo sapiens
1395 Laura Do Souto Ferreira Dec 14, 2022
GSE209728
Affymetrix CytoScan HD data on neuroblastoma cell lines
  • Link icon Homo sapiens
16 Susanne Marie Fransson Nov 10, 2022
GSE211577
Fetal genetic findings for fetal growth restriction without structural malformations at a territory referral center: 10-year experience
  • Link icon Homo sapiens
31 Xiaoqing Wu Sep 20, 2022
GSE212870
Array46 750k test is an in-depht analysis to detect chromosomal alterations, CNVs and SNPs
  • Link icon Homo sapiens
4 consuelo salas Sep 10, 2022
GSE205269
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults [SNP]
  • Link icon Homo sapiens
15 Cristina Mecucci Aug 17, 2022