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chromosomes human, pair 11
(tissue)
Summary
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Body Atlas
Curated Studies
Most Correlated Studies
OMIM - Congenital chromosomal disease
OMIM - Congenital disorder
Acute myeloid leukemia by karyotype and by discrete mutation
Bone marrow gene expression of pediatric acute lymphoblastic leukemia
Bone marrow or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
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Sustained endocrine profiles of a girl with WAGR syndrome.
Haplotype frequency distribution for 7 microsatellites in chromosome 8 and 11 in relation to the met…
Molecular and clinical characterization of patients with a ring chromosome 11.
Clinical, histologic, and genetic features of mesothelioma in a 7-year-old child.
Tissue-specific regulatory regions of the PTH gene localized by novel chromosome 11 rearrangement br…
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A Positional Cloning Study on Schizophrenia
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
PGS Using Microarray in IVF Patients With Repeated Implantation Failure
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