Genomic imprinting and Beckwith-Wiedemann syndrome

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Campo DC	Valor	Lengua/Idioma
dc.contributor.author	Hatada, I.	es
dc.contributor.author	Mukai, T.	es
dc.date.accessioned	2011-02-22T11:19:57Z	-
dc.date.available	2011-02-22T11:19:57Z	-
dc.date.issued	2000	-
dc.identifier.issn	0213-3911	es
dc.identifier.uri	http://hdl.handle.net/10201/19270	-
dc.description.abstract	Genomic imprinting is the parental-allelespecific expression of genes. Beckwith-Wiedemann syndrome (BWS), a congenital overgrowth syndrome with increased risk of childhood tumors, is one of the well-known diseases caused by imprinted genes. The imprinted genes causing BWS are discussed in this review.	es
dc.format	application/pdf	es
dc.format.extent	4	es
dc.language	eng	es
dc.publisher	Murcia : F. Hernández	es
dc.relation.ispartof	Histology and histopathology	es
dc.rights	info:eu-repo/semantics/openAccess	es
dc.subject	Genomic imprinting	es
dc.subject	Beckwith Wiedemann syndrome	es
dc.subject.other	CDU::5 - Ciencias puras y naturales::57 - Biología::577 - Bioquímica. Biología molecular. Biofísica	es
dc.title	Genomic imprinting and Beckwith-Wiedemann syndrome	es
dc.type	info:eu-repo/semantics/article	es
Aparece en las colecciones:	Vol.15, nº 1 (2000)

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