(Q43204600)

16 November 2017

0 references

The two-domain hypothesis in Beckwith-Wiedemann syndrome (English)

1 reference

16 November 2017

A P Feinberg

1

1 reference

PMCID

381397

16 November 2017

language of work or name

English

0 references

publication date

1 September 2000

1 reference

Journal of Clinical Investigation

16 November 2017

1 reference

16 November 2017

106

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16 November 2017

6

1 reference

16 November 2017

739-740

1 reference

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

16 November 2017

1 reference

12 December 2020

Relaxation of imprinted genes in human cancer.

1 reference

12 December 2020

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

1 reference

12 December 2020

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 reference

12 December 2020

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

1 reference

12 December 2020

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI10911

1 reference

16 November 2017

1 reference

16 November 2017

1 reference

PMCID

381397