genomic mutation

  • 111Mucovicidose — Mucoviscidose Mucoviscidose Autre nom Fibrose kystique du pancréas Référence MIM …

    Wikipédia en Français

  • 112Mucoviscidose — Pour les articles homonymes, voir CF. Mucoviscidose Référence MIM 219700 Transmission Autosomique récessive Chromosome …

    Wikipédia en Français

  • 113Mucovisidose — Mucoviscidose Mucoviscidose Autre nom Fibrose kystique du pancréas Référence MIM …

    Wikipédia en Français

  • 114Test de la sueur — Mucoviscidose Mucoviscidose Autre nom Fibrose kystique du pancréas Référence MIM …

    Wikipédia en Français

  • 115Anthropology and Archaeology — ▪ 2009 Introduction Anthropology       Among the key developments in 2008 in the field of physical anthropology was the discovery by a large interdisciplinary team of Spanish and American scientists in northern Spain of a partial mandible (lower… …

    Universalium

  • 116syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …

    Medical dictionary

  • 117Human genome — The human genome is the genome of Homo sapiens , which is stored on 23 chromosome pairs. Twenty two of these are autosomal chromosome pairs, while the remaining pair is sex determining. The haploid human genome occupies a total of just over 3… …

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  • 118Long non-coding RNA — Long noncoding RNAs (long ncRNAs) are generally considered (somewhat arbitrarily) as non protein coding transcripts longer than 200 nucleotides. This limit is due to practical considerations including the separation of RNAs in common experimental …

    Wikipedia

  • 119genetic disease, human — Introduction       any of the diseases and disorders that are caused by mutations in one or more genes (gene).       With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization …

    Universalium

  • 120Copy-number variation — This gene duplication has created a copy number variation. The chromosome now has two copies of this section of DNA, rather than one. Copy number variations (CNVs) a form of structural variation are alterations of the DNA of a genome that results …

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