Search
Descriptor English: Chromosome Fragile Sites
Descriptor Spanish: Sitios Frágiles del Cromosoma
Descriptor sitios frágiles de los cromosomas
Entry term(s) sítios cromosómicos frágiles
sítios frágiles cromosómicos
Scope note: Loci específicos que se muestran durante la CARIOTIPIFICACIÓN como una brecha (tramo no condensado a mayor aumento) en un brazo de la CROMÁTIDE después de cultivar las células en condiciones específicas. Estos sitios se asocian con un aumento de la FRAGILIDAD CROMOSÓMICA. Se clasifican como frecuentes o raros, y según las condiciones específicas de cultivo en las que se desarrollan. Los loci de los sitios frágiles se denominan con las "FRA" seguidas por una designación del cromosoma específico y una letra que se refiere al sitio frágil de ese cromosoma (p. ej., FRAXA se refiere al sitio frágil A en el cromosoma X. Es un sitio frágil, raro y sensible al ácido fólico que se asocia al SÍNDROME DEL CROMOSOMA X FRÁGIL).
Descriptor Portuguese: Sítios Frágeis do Cromossomo
Descriptor French: Sites fragiles de chromosome
Tree number(s): G05.360.340.024.189.610
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D043283
Scope note: Specific loci that show up during KARYOTYPING as a gap (an uncondensed stretch in closer views) on a CHROMATID arm after culturing cells under specific conditions. These sites are associated with an increase in CHROMOSOME FRAGILITY. They are classified as common or rare, and by the specific culture conditions under which they develop. Fragile site loci are named by the letters "FRA" followed by a designation for the specific chromosome, and a letter which refers to which fragile site of that chromosome (e.g. FRAXA refers to fragile site A on the X chromosome. It is a rare, folic acid-sensitive fragile site associated with FRAGILE X SYNDROME.)
Allowable Qualifiers: DE effets des médicaments et des substances chimiques
ES éthique
GE génétique
IM immunologie
PH physiologie
RE effets des radiations
Related: Expansion de séquence répétée de l'ADN MeSH
Fragilité des chromosomes MeSH
Syndrome du chromosome X fragile MeSH
DeCS ID: 38395
Unique ID: D043283
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2004/01/01
Date of Entry: 2003/07/09
Revision Date: 2013/07/09
Sites fragiles de chromosome - Preferred
Concept UI M0004412
Preferred term Sites fragiles de chromosome



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey