scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1028842591 |
P356 | DOI | 10.1038/360492A0 |
P698 | PubMed publication ID | 1448175 |
P2093 | author name string | Davies K | |
P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome | Q24337580 | ||
Monoallelic expression of the human H19 gene | Q28184725 | ||
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region | Q28208127 | ||
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis | Q31165084 | ||
Uniparental paternal disomy in Angelman's syndrome | Q33244469 | ||
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. | Q34680586 | ||
DNA deletion and its parental origin in Angelman syndrome patients | Q41135500 | ||
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression | Q67482957 | ||
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression | Q67510275 | ||
P433 | issue | 6403 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 492 | |
P577 | publication date | 1992-12-01 | |
1992-12-03 | |||
P1433 | published in | Nature | Q180445 |
P1476 | title | Imprinting and splicing join together | |
P478 | volume | 360 |
Q60065191 | Imprinting makes its mark | cites work | P2860 |
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