De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation

BACKGROUND: Marfan syndrome (MFS) is an autosomal dominant disease caused by mutations in the Fibrillin (FBN)1 gene and characterized by disorders in the cardiovascular, skeletal, and visual systems. The diversity of mutations and phenotypic heterogeneity of MFS make prenatal molecular diagnoses dif...

Deskribapen osoa

Xehetasun bibliografikoak
Egile Nagusiak: Wang, Shuling, Niu, Ziru, Wang, Hui, Ma, Minyue, Zhang, Wei, Wang, Shu Fang, Wang, Jun, Yan, Hong, Liu, Yifan, Duan, Na, Zhang, Xiandong, Yao, Yuanqing
Formatua: Online Artikulua Texto
Hizkuntza:English
Argitaratua: International Scientific Literature, Inc. 2017
Gaiak:
Lab/In Vitro Research
Sarrera elektronikoa:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498129/
https://www.ncbi.nlm.nih.gov/pubmed/28650953
http://dx.doi.org/10.12659/MSM.904546

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498129/
https://www.ncbi.nlm.nih.gov/pubmed/28650953
http://dx.doi.org/10.12659/MSM.904546

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