L'empreinte génomique : paradigmes du syndrome de Beckwith-Wiedemann et du syndrome de Turner

Hamelin, Catherine

dc.contributor.advisor	Deal, Cheri L.
dc.contributor.author	Hamelin, Catherine
dc.date.accessioned	2023-09-29T14:46:32Z
dc.date.available	2023-09-29T14:46:32Z
dc.date.issued	2001
dc.date.submitted	2001
dc.identifier.uri	http://hdl.handle.net/1866/29475
dc.subject	Épigénétique
dc.subject	Méthylation
dc.subject	Origine parentale
dc.subject	Chromosome II
dc.subject	Chromosome X
dc.subject	Jumeaux monozygotiques
dc.subject	Microsatellites
dc.subject	GH
dc.subject	IGF2
dc.subject	H19
dc.title	L'empreinte génomique : paradigmes du syndrome de Beckwith-Wiedemann et du syndrome de Turner
dc.type	Thèse ou mémoire / Thesis or Dissertation
etd.degree.discipline	Sciences biomédicales	fr
etd.degree.grantor	Université de Montréal	fr
etd.degree.level	Maîtrise / Master's
etd.degree.name	M. Sc.
dcterms.description	Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.	fr
dcterms.language	fra

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