interstitial deletion

interstitial deletion
loss of a segment within a chromosome arm. See illustration at aberration.

Medical dictionary. 2011.

Игры ⚽ Нужна курсовая?

Look at other dictionaries:

  • Deletion (genetics) — Deletion on a chromosome In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is missing. Deletion is the loss of …   Wikipedia

  • Deletion — Loss of a segment of DNA from a chromosome (and hence from the genome). The first human chromosome deletion was detected in 1963 by Jerome Lejeune and his colleagues in Paris. They discovered loss of part of 5p, the short (p) arm of chromosome 5 …   Medical dictionary

  • Chromosome 5q deletion syndrome — Classification and external resources Photomicrograph of bone marrow showing abnormal mononuclear megakaryocytes typical of 5q syndrome ICD O: M …   Wikipedia

  • Smith–Magenis syndrome — Classification and external resources ICD 9 758.33 OMIM 182290 DiseasesDB …   Wikipedia

  • Smith-Magenis syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 31737 ICD10 = ICD9 = ICD9|758.33 ICDO = OMIM = 182290 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Smith Magenis Syndrome (SMS) is a developmental disorder that affects many parts… …   Wikipedia

  • Gap-43 protein — Growth associated protein 43 Identifiers Symbols GAP43; B 50; PP46 External IDs OMIM …   Wikipedia

  • Glypican 3 — Glypican 3, also known as GPC3, is a human gene.cite web | title = Entrez Gene: GPC3 glypican 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2719| accessdate = ] cite journal | author = Jakubovic BD,… …   Wikipedia

  • Adenosine deaminase — (also known as ADA) is an enzyme (EC number|3.5.4.4) involved in purine metabolism. It is needed for the breakdown of adenosine from food and for the turnover of nucleic acids in tissues.ReactionsADA irreversibly deaminates adenosine, converting… …   Wikipedia

  • RPE (gene) — Ribulose 5 phosphate 3 epimerase, also known as RPE, is a human gene.cite web | title = Entrez Gene: RPE ribulose 5 phosphate 3 epimerase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6120| accessdate = ] …   Wikipedia

  • WAGR syndrome — Wilms tumour (see nephroblastoma), aniridia, genitourinary abnormalities, and mental retardation: a condition due to a deletion of part of the short arm of chromosome 11. * * * a syndrome of Wilms tumor, aniridia, genitourinary abnormalities or… …   Medical dictionary

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”