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QuickView for chromosome 17


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 or peripheral blood mononuclear cells of pediatric acute myeloid leukemia patients
  5. Gene expression in neuroblastomas with recurrent genomic alterations
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Literature

Most Relevant Literature

  1. How a paternal uniparental isodisomy of chromosome 17 leads to autosomal recessive limb-girdle muscu…
  2. Characterization and prognostic implication of 17 chromosome abnormalities in myelodysplastic syndro…
  3. Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the ad…
  4. Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation.
  5. Mosaic RAI1 variant in a Smith-Magenis syndrome patient with total anomalous pulmonary venous return…
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Clinical Trials

Most Relevant Clinical Trials

  1. Efficiency of Comprehensive Chromosomal Testing of Trophectoderm Biopsies of Blastocysts in In Vitro…
  2. Non-Invasive Chromosomal Evaluation of 22q11.2
  3. Relationship Between Plasma Concentration of Hydroxyprogesterone Caproate (17-OHPC) and Preterm Birt…
  4. The eXtroardinarY Babies Study: Natural History of Health and Neurodevelopment in Infants and Young …
  5. Endocrine, Metabolic, Cardiovascular and Immunological Aspects of Sex Chromosome Abnormalities in Re…
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