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Results 1 - 10 of 31 for Definitions
  1. Epilepsy-aphasia spectrum 
    ... Auvin S. International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position ... by the ILAE Task Force on Nosology and Definitions. Epilepsia. 2022 Jun;63(6):1398-1442. doi: ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  2. Is intelligence determined by genetics?: MedlinePlus Genetics 
    ... be defined and measured in different ways. Most definitions of intelligence include the ability to learn from ...
    https://medlineplus.gov/genetics/understanding/traits/intelligence - Genetics
  3. 1p36 deletion syndrome 
    ... of hematological neoplasias with 1p36 rearrangements allows the definition of a cluster of 2.5 Mb included ...
    https://medlineplus.gov/genetics/condition/1p36-deletion-syndrome - Genetics
  4. What is precision medicine?: MedlinePlus Genetics 
    According to the Precision Medicine Initiative, precision medicine is "an emerging approach for disease treatment and prevention that takes into account individual ...
    https://medlineplus.gov/.../precisionmedicine/definition - Genetics
  5. Autism spectrum disorder 
    ... many affected individuals fall outside of the strict definitions of the narrower diagnoses, and their intellectual and ...
    https://medlineplus.gov/genetics/condition/autism-spectrum-disorder - Genetics
  6. TYR gene 
    ... Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype. Hum Genet. 2003 Nov;113( ...
    https://medlineplus.gov/genetics/gene/tyr - Genetics
  7. Ring chromosome 14 syndrome 
    ... G. The ring 14 syndrome: clinical and molecular definition. Am J Med Genet A. 2009 Jun;149A( ...
    https://medlineplus.gov/.../condition/ring-chromosome-14-syndrome - Genetics
  8. 2q37 deletion syndrome 
    ... analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes. J ...
    https://medlineplus.gov/genetics/condition/2q37-deletion-syndrome - Genetics
  9. CHST3 gene 
    ... K, Robertson SP. Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype. Am J Med Genet A. ...
    https://medlineplus.gov/genetics/gene/chst3 - Genetics
  10. Potocki-Lupski syndrome 
    ... S, Sgro M, Walz K, Mendoza-Londono R. Definition of a critical genetic interval related to kidney ...
    https://medlineplus.gov/genetics/condition/potocki-lupski-syndrome - Genetics
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