Monosomy — Classification and external resources ICD 10 Q93, Q96 MeSH … Wikipedia
Monosomy 9p — Classification and external resources OMIM 158170 Monosomy 9p (also known as Alfi s Syndrome or simply 9P ) is a rare chromosomal disorder in which there is deletion (monosomy) of a portion of chromosome 9. Symptoms include microgenitalia, mental … Wikipedia
Monosomy 14 — Monosomy is a form of aneuploidy with the presence of only one chromosome (instead of the typical two in humans) from a pair, which affects chromosome 14. Fetuses with monosomy 14 are not viable.[1] Only mosaic cases exist and these usually… … Wikipedia
monosomy — monosomy. См. гаплосомия. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
Monosomy 18p — is the deletion of all or part of the short arm of chromosome 18. Symptoms include mental retardation and several dysmorphic features. It was first described by Jean de Grouchy in 1963.References* … Wikipedia
monosomy — noun see monosomic … New Collegiate Dictionary
monosomy — Situation in a normally diploid cell or organism in which one or more of the homologous chromosome pairs is represented by only one chromosome of the pair. For example, sex determination in grasshoppers depends on the fact that females are XX and … Dictionary of molecular biology
monosomy — See monosomic. * * * … Universalium
monosomy — noun A genetic disorder with the presence of only one chromosome (instead of the typical two in humans) from a pair. See Also: aneuploidy … Wiktionary
monosomy — n. having only one copy of a particular chromosome instead of the normal two copies … English contemporary dictionary
