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  2. Chromosomal translocation - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_translocation

    The former results in a chromosomal abnormality featured in all cells of the offspring, as in translocation carriers. Somatic translocations, on the other hand, result in abnormalities featured only in the affected cell and its progenitors, as in chronic myelogenous leukemia with the Philadelphia chromosome translocation.

  3. Mouse models of Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Mouse_models_of_Down_syndrome

    The Dp(16)1Yu model (also referred to as Dp(16)1Yey) contains a partial duplication of the mouse chromosome 16 (MMU16). Unlike the Ts65Dn model, Dp(16)1Yu contains a duplication of only the parts of chromosome 16 that are homologous to human chromosome 21. This makes the Dp(16)1Yu model a more genetically accurate representation of Down Syndrome.

  4. 22q13 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/22q13_deletion_syndrome

    22q13 deletion syndrome, known as Phelan–McDermid syndrome (PMS), is a genetic disorder caused by deletions or rearrangements on the q terminal end (long arm) of chromosome 22.

  5. Deletion (genetics) - Wikipedia

    en.wikipedia.org/wiki/Deletion_(genetics)

    Deletions are responsible for an array of genetic disorders, including some cases of male infertility, two thirds of cases of Duchenne muscular dystrophy, [1] and two thirds of cases of cystic fibrosis (those caused by ΔF508). [9] Deletion of part of the short arm of chromosome 5 results in Cri du chat syndrome. [1]

  6. Ring chromosome 20 syndrome - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_20_syndrome

    Ring chromosome 20, ring-shaped chromosome 20 or r(20) syndrome is a rare human chromosome abnormality where the two arms of chromosome 20 fuse to form a ring chromosome.The syndrome is associated with epileptic seizures, behaviour disorders and intellectual disability.

  7. Beckwith–Wiedemann syndrome - Wikipedia

    en.wikipedia.org/wiki/Beckwith–Wiedemann_syndrome

    Beckwith–Wiedemann syndrome (/ ˈ b ɛ k ˌ w ɪ θ ˈ v iː d ə. m ə n /; abbreviated BWS) is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features.

  8. Jeffrey Dahmer - Wikipedia

    en.wikipedia.org/wiki/Jeffrey_Dahmer

    Jeffrey Lionel Dahmer (/ ˈ d ɑː m ər /; May 21, 1960 – November 28, 1994), also known as the Milwaukee Cannibal or the Milwaukee Monster, [4] was an American serial killer and sex offender who killed and dismembered seventeen males between 1978 and 1991. [5]

  9. XXXY syndrome - Wikipedia

    en.wikipedia.org/wiki/XXXY_syndrome

    XXXY syndrome is a genetic condition characterized by a sex chromosome aneuploidy, where individuals have two extra X chromosomes. [2] People in most cases have two sex chromosomes: an X and a Y or two X chromosomes.

  1. Related searches partial trisomy 10q results range table for dogs 4 to 9 months

    partial trisomy 10q results range table for dogs 4 to 9 months old