179 series
Export
<<< of 9>>>
Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterCYCHP
GSE240546
Comparison of CNV in 6 ostosarcoma cell lines
6 Chia-Ho Cheng Nov 22, 2023
GSE230532
Prenatal Diagnosis and Clinical Analysis of Talipes Equinovarus by Chromosomal Microarray Analysis
131 Xiaorui Xie Oct 22, 2023
GSE197838
Affymetrix SNP array data for acute lymphoblastic leukemia samples
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
5 Yanting Que Sep 27, 2023
GSE240611
Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications
26 Hongguo Zhang Aug 14, 2023
GSE178421
Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma [Cytoscan]
23 Joan Enric Ramiz-Zaldivar Jun 05, 2023
GSE178427
Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma
35 Joan Enric Ramiz-Zaldivar Jun 05, 2023
GSE233748
Affymetrix SNP array data for an INAD patient
1 yongxue lv May 31, 2023
GSE207887
Chromosomal abnormalities of 564 miscarriages
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?
129 su linjuan Apr 30, 2023
GSE213813
Affymetrix SNP array data for induced pluripotent stem cell line
4 Yolanda Aguilera Feb 15, 2023
GSE223242
Genetic analysis, ultrasound phenotype, and pregnancy outcome of fetuses with Xp22.33 or Yp11.32 microdeletion
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
1395 Laura Do Souto Ferreira Dec 14, 2022
GSE209728
Affymetrix CytoScan HD data on neuroblastoma cell lines
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
31 Xiaoqing Wu Sep 20, 2022
GSE212870
Array46 750k test is an in-depht analysis to detect chromosomal alterations, CNVs and SNPs
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]
15 Cristina Mecucci Aug 17, 2022
GSE205270
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults
108 Cristina Mecucci Aug 17, 2022
GSE208389
Retrospective study of 186 fetuses with sex chromosomal copy number variations
185 Haiwei Wang Jul 29, 2022
GSE208291
Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis using ultrasound in Southern China
7 Hailong Huang Jul 16, 2022