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chromosomes human, pair 10
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Summary
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Body Atlas
Curated Studies
Most Correlated Studies
OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
Bone marrow or peripheral blood from pediatric relapsed acute myeloid leukemia (AML) patients
Gene expression in neuroblastomas with recurrent genomic alterations
Molecular signature of the t(12;14) subgroup of uterine leiomyomata
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Role of DNA secondary structures in fragile site breakage along human chromosome 10.
Detailed characterization of alterations of chromosomes 7, 9, and 10 in glioblastomas as assessed by…
The phosphatase and tensin homologue deleted on chromosome 10 mediates radiosensitivity in head and …
A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequ…
Ring chromosome 10: report on two patients and review of the literature.
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Turner Syndrome: Genotype and Phenotype
Evaluation of Patients With Unresolved Chromosome Abnormalities
Reduced Intensity Donor Stem Cell Transplant in Treating Patients With High Risk Acute Lymphocytic L…
Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
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