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QuickView for chromosomes human, pair 9 (tissue)


Body Atlas

 
 

Curated Studies

Most Correlated Studies

  1. OMIM - Congenital chromosomal disease
  2. OMIM - Congenital disorder
  3. Acute myeloid leukemia by karyotype and by discrete mutation
  4. Bone marrow gene expression of pediatric acute lymphoblastic leukemia
  5. Bone marrows from acute myleoid leukemia (AML) patients grouped by chromosomal abnormalities
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Literature

Most Relevant Literature

  1. Intratumoral heterogeneity of chromosome 9 loss and CDKN2A (p16) protein expression in a morphologic…
  2. Detailed characterization of alterations of chromosomes 7, 9, and 10 in glioblastomas as assessed by…
  3. Mapping of Char10, a novel malaria susceptibility locus on mouse chromosome 9.
  4. Heteromorphic variants of chromosome 9.
  5. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryp…
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Clinical Trials

Most Relevant Clinical Trials

  1. Evaluation of Patients With Unresolved Chromosome Abnormalities
  2. A Positional Cloning Study on Schizophrenia
  3. Reduced Intensity Donor Stem Cell Transplant in Treating Patients With High Risk Acute Lymphocytic L…
  4. Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
  5. Mutation Screening and Translocation Detection of DISC1 Gene in Schizophrenia
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