Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19-Independent Pathway

KW Brown, AJ Villar, W Bickmore… - Human molecular …, 1996 - academic.oup.com
Abstract The Beckwith-Wiedemann syndrome (BWS) is genetically linked to chromosome
11p15. 5, and a variety of observations suggest that deregulation of imprinted genes in this …
被引用次数：154 相关文章

[引用][C] Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through and H19-independent pathway

B KW - Hum Mol Genet, 1996 - cir.nii.ac.jp
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression
through and H19-independent pathway | CiNii Research CiNii 国立情報学研究所 学術情報 …

[引用][C] Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

KW Brown, AJ Villar, W Bickmore… - Human Molecular …, 1996 - elibrary.ru

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

KW Brown, AJ Villar, W Bickmore… - Human molecular …, 1996 - pubmed.ncbi.nlm.nih.gov
The Beckwith-Wiedemann syndrome (BWS) is genetically linked to chromosome 11p15. 5,
and a variety of observations suggest that deregulation of imprinted genes in this region is …

Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19-Independent Pathway.

KW Brown, AJ Villar, W Bickmore… - Human Molecular …, 1996 - search.ebscohost.com
Abstract The Beckwith-Wiedemann syndrome (BWS) is genetically linked to chromosome
11p15. 5, and a variety of observations suggest that deregulation of imprinted genes in this …
[PDF] archive.org

[PDF][PDF] Imprinting mutation in the Beckwith–Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

KW Brown, AJ Villar, W Bickmore… - Human Molecular …, 1996 - scholar.archive.org
The genetic regulation of genomic imprinting is of considerable importance for normal
development and for genetic disease. Close physical clustering appears to be an important …

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.

KW Brown, AJ Villar, W Bickmore… - Human Molecular …, 1996 - europepmc.org
The Beckwith-Wiedemann syndrome (BWS) is genetically linked to chromosome 11p15. 5,
and a variety of observations suggest that deregulation of imprinted genes in this region is …

[引用][C] Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

KW BROWN, AJ VILLAR, W BICKMORE… - Human molecular …, 1996 - pascal-francis.inist.fr
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2
expression through an H19-independent pathway CNRS Inist Pascal-Francis CNRS Pascal …
[PDF] psu.edu

[PDF][PDF] Imprinting mutation in the Beckwith–Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

KW Brown, AJ Villar, W Bickmore… - Human Molecular …, 1996 - Citeseer
The genetic regulation of genomic imprinting is of considerable importance for normal
development and for genetic disease. Close physical clustering appears to be an important …

[引用][C] Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

KW BROWN, AJ VILLAR… - Human molecular …, 1996 - Oxford University Press