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OMIM - Congenital disorder
Human iPSCs with chromosome 7 deletion (chr7q) and self-corrected by extra chromosome 7 gain
OMIM - Congenital chromosomal disease
Mouse Phenotypes - Congenital disorder
Wilms tumors from different syndrome types and WT1 mutation statuses
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Diffuse leptomeningeal neuroepithelial tumor: 9 pediatric cases with chromosome 1p/19q deletion stat…
Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutatio…
Nodal marginal zone B cell lymphoma with prominent follicular colonization with deletion of chromoso…
Molecular characterization of Xp chromosome deletion in a fertile cow.
Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a …
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Unrelated And Partially Matched Related Donor PSCT w/ T Cell Receptor (TCR) αβ Depletion for Patient…
Phase I/II Study of Combination of Sorafenib, Vorinostat, and Bortezomib for the Treatment of Acute …
Comparison Between Fotemustin to Intensive Surveillance in Patients With High Risk Uveal Melanoma
LENA-LMA-5:Lenalidomide in Acute Myeloid Leukemia (AML)
UTHealth Turner Syndrome Research Registry
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