Functional consequences of copy number variants in miscarriage

BACKGROUND: The presence of unique copy number variations (CNVs) in miscarriages suggests that their integral genes have a role in maintaining early pregnancy. In our previous work, we identified 19 unique CNVs in ~40% of studied euploid miscarriages, which were predominantly familial in origin. In...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Mol Cytogenet
Egile Nagusiak: Wen, Jiadi, Hanna, Courtney W, Martell, Sally, Leung, Peter CK, Lewis, Suzanne ME, Robinson, Wendy P, Stephenson, Mary D, Rajcan-Separovic, Evica
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2015
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4324423/
https://ncbi.nlm.nih.gov/pubmed/25674159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-015-0109-8
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak