A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

ataxie spinocérébelleuse type 26

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

delete from a fund

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

radier d'un fonds

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

A rare chromosomal anomaly syndrome resulting from a partial deletion of the long arm of chromosome 10. The disease has a highly variable phenotype with principle characteristics of developmental delay (usually of language and speech), variable cogni

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

monosomie non distale 10q

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome de microdélétion 9p13

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

D'autres ont cherché : deletion from autosomes other deletions from the autosomes delete from a fund deletion from ring Deletion from autosomes

datacenter (1): www.wordscope.fr (v4.0.br)

'Deletion from autosomes' ->

Date index: 2023-07-13