Imprinting and splicing join together

scientific article published on December 3, 1992

Imprinting and splicing join together is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1028842591
P356DOI10.1038/360492A0
P698PubMed publication ID1448175

P2093author name stringDavies K
P2860cites workParental imprinting of the mouse H19 geneQ22122365
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndromeQ24337580
Monoallelic expression of the human H19 geneQ28184725
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical regionQ28208127
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisQ31165084
Uniparental paternal disomy in Angelman's syndromeQ33244469
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.Q34680586
DNA deletion and its parental origin in Angelman syndrome patientsQ41135500
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome regionQ44185908
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expressionQ67482957
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expressionQ67510275
P433issue6403
P407language of work or nameEnglishQ1860
P304page(s)492
P577publication date1992-12-01
1992-12-03
P1433published inNatureQ180445
P1476titleImprinting and splicing join together
P478volume360

Reverse relations

Q60065191Imprinting makes its markcites workP2860

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