Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction-Reference-Cited by-同舟云学术

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Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction

Published:2012-12-14 Issue:2 Volume:50 Page:99-103
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

De Crescenzo Agostina,Sparago Angela,Cerrato Flavia,Palumbo Orazio,Carella Massimo,Miceli Marco,Bronshtein Moshe,Riccio Andrea,Yaron Yuval

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Imprinted lncRNA KCNQ1OT1 regulates CDKN1C expression through promoter binding and chromatin folding in pigs;Gene;2024-09

2. Human Reproduction and Disturbed Genomic Imprinting;Genes;2024-01-26

3. Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum;Genes;2022-10-16

4. CDKN1Chyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inheritedKCNQ1OT1:TSS-DMR;Journal of Medical Genetics;2022-07-29

5. A 132 bp deletion affecting theKCNQ1OT1gene associated with Silver-Russell syndrome clinical phenotype;Journal of Medical Genetics;2022-06-30

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