tetrasomy

tetrasomy
tet·ra·so·my

English syllables. 2014.

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  • Tetrasomy 18p — is a rare genetic disease where the short arm of chromosome 18 appears not just two times in a base pair, but four times. The additional chromosome is called a marker or an isochromosome.External links*… …   Wikipedia

  • tetrasomy — tet·ra·so·my (tetґrə so″me) [tetra + Gr. sōma body] the presence of two additional chromosomes of one type in an otherwise diploid cell (2n + 2). tetrasomic adj …   Medical dictionary

  • tetrasomy — noun see tetrasomic I …   Useful english dictionary

  • tetrasomy 12p — Pallister Killian syndrome …   Medical dictionary

  • 48, XXXX — Infobox Disease Name = XXXX syndrome Caption = DiseasesDB = 32550 ICD10 = ICD10|Q|97|1|q|90 ICD9 = ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = XXXX syndrome (also called tetrasomy X, quadruple X, or 48, XXXX) is a rare… …   Wikipedia

  • Aneuploidy — Classification and external resources ICD 10 Q90 Q98 ICD 9 …   Wikipedia

  • List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… …   Wikipedia

  • Pallister-Killian syndrome — Infobox Disease Name = Pallister Killian syndrome Caption = ICD10 = ICD10|Q|99|8|q|90 ICD9 = ICD9|758.5 OMIM = 601803 Pallister Killian syndrome (also tetrasomy 12p mosaicism or Pallister mosaic aneuploidy syndrome) is an extremely rare genetic… …   Wikipedia

  • Chromosome abnormality — The three major single chromosome mutations; deletion (1), duplication (2) and inversion (3) …   Wikipedia

  • Синдром Клайнфельтера — Кариотип …   Википедия

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