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Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Bone marrow or peripheral blood from pediatric relapsed acute myeloid leukemia (AML) patients
Molecular signature of the t(12;14) subgroup of uterine leiomyomata
Foreskin fibroblast and derived iPSC expression of normal individuals and patients with Klinefelters
Striata from Klinefelter syndrome mice
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Cobalamin C defect: natural history, pathophysiology, and treatment.
Integrative genomic analyses of the histamine H1 receptor and its role in cancer prediction.
Hypoxia-induced modulation of PTEN activity and EMT phenotypes in lung cancers.
Left ventricular hypertrophy caused by a novel nonsense mutation in FHL1.
Modulation of chromosome damage localization by DNA replication timing.
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Chromosome 18 Clinical Research Center
The Clinical Study of Sex Chromosome Variants
Efficiency of Comprehensive Chromosomal Testing of Trophectoderm Biopsies of Blastocysts in In Vitro…
Non-invasive Placental Chromosome Exploration of Intrauterine Growth Restriction
Trisomy of Chromosome 21 Diagnosis by High Output Sequencing
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