Copy number variation analysis of 18,000 fetuses in southern China

Uniparental disomy: expanding the clinical and molecular phenotypes of whole chromosomes

Affymetrix SNP array data for T-cell acute lymphoblastic leukemia samples

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]

A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias

K-562 cell lines

Comparison of CNV in 6 ostosarcoma cell lines

Prenatal Diagnosis and Clinical Analysis of Talipes Equinovarus by Chromosomal Microarray Analysis

Affymetrix SNP array data for acute lymphoblastic leukemia samples

Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele: a single tertiary center experience

Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications

Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma [Cytoscan]

Global genetic profiling of a pediatric series of T-cell lymphoblastic lymphoma

Affymetrix SNP array data for an INAD patient

Chromosomal abnormalities of 564 miscarriages

Can non-invasive prenatal screening based on cell-free fetal DNA be utilized to assess chromosome abnormalities in fetuses with increased Nuchal Translucency?

Affymetrix SNP array data for induced pluripotent stem cell line

Genetic analysis, ultrasound phenotype, and pregnancy outcome of fetuses with Xp22.33 or Yp11.32 microdeletion

Double-deletion of 1p32 defines ultra-high-risk myeloma, but monoallelic del(1p32) remains a strong prognostic factor

Affymetrix CytoScan HD data on neuroblastoma cell lines