Uniparental paternal disomy in a genetic cancer-predisposing syndrome. - Wikidata - awgldk - TriplyDB

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

http://www.wikidata.org/entity/Q34535432

about

Mapping of the human casein kinase II catalytic subunit genes: two loci carrying the homologous sequences for the alpha subunit Risk of breast and prostate cancer is not associated with increased homozygosity in outbred populations Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy The human silent information regulator (Sir)2 homologue hSIRT3 is a mitochondrial nicotinamide adenine dinucleotide-dependent deacetylase Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation Integrative genomic analysis reveals extended germline homozygosity with lung cancer risk in the PLCO cohort Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology Monoallelic expression of the human H19 gene Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11 An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome Mouse homologues of human hereditary disease.Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers The new dysmorphology: application of insights from basic developmental biology to the understanding of human birth defects.Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2.'Deletion rescue' by mitotic 11q uniparental disomy in a family with recurrence of 11q deletion Jacobsen syndrome.Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).Sotos syndrome: a study of the diagnostic criteria and natural history.Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.Inherited renal cancer.Wilms tumor genetics.Differential expression of insulin-like growth factors I and II (IGF I and II), mRNA, peptide and binding protein 1 during mouse palate development: comparison with TGF beta peptide distribution Molecular adrenocortical tumourigenesis.Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans.cgaTOH: extended approach for identifying tracts of homozygosity.Genomic imprinting proposed as a surveillance mechanism for chromosome loss.Advances in genetics American College of Medical Genetics statement of diagnostic testing for uniparental disomy Clonality and evolutionary history of rhabdomyosarcoma A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci Uniparental disomy for chromosome 16 in humans.Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.Normal phenotype with paternal uniparental isodisomy for chromosome 21.

P2860

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P2860

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

http://www.wikidata.org/entity/Q34535432

description

1991 nî lūn-bûn

@nan

1991 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

1991 թվականի հունիսին հրատարակված գիտական հոդված

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1991年の論文

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1991年論文

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1991年論文

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1991年論文

@zh-hk

1991年論文

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1991年論文

@zh-tw

1991年论文

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name

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@ast

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@en

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

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type

label

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@ast

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@en

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@nl

prefLabel

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@ast

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@en

Uniparental paternal disomy in a genetic cancer-predisposing syndrome.

@nl

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Beldjord C

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Bonaiti-Pellié C

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Chehensse V

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Henry I

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Junien C

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10.1038/351665A0

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