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chromosomes human, pair 12
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Curated Studies
Most Correlated Studies
OMIM - Congenital chromosomal disease
Bone marrow gene expression of pediatric acute lymphoblastic leukemia
Molecular signature of the t(12;14) subgroup of uterine leiomyomata
Trisomy 21 and 13 expression from fetal cerebrum, cerebellum, and heart
Colorectal cancer and embryonic kidney cells with CASC8 enhancer E7 deletion
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Literature
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Cellular consequences of small supernumerary marker chromosome derived from chromosome 12: mosaicism…
ETV6::ACSL6 fusion gene in myeloid malignancies with eosinophilia: a report of two cases with t(5;12…
Replication stress causes delayed mitotic entry and chromosome 12 fragility at the ANKS1B large neur…
Rheumatoid arthritis in Latin Americans enriched for Amerindian ancestry is associated with loci in …
Histopathological Correlation of Chromosome 12 Polysomy by Fluorescence in Situ Hybridization in Adi…
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Reduced Intensity Donor Stem Cell Transplant in Treating Patients With High Risk Acute Lymphocytic L…
Validation of the Accuracy of DNA Fingerprinting Using Polar Bodies and Embryonic Cells
Phase I Study of Oral BAY 1217389 in Combination With Intravenous Paclitaxel
The Association Between Telomere Length and Propofol Dose in Anesthesia-induction
A Positional Cloning Study on Schizophrenia
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