Prenatal Diagnosis and Genetic Analysis of a Fetus with Joubert Syndrome.

Conclusion: Our study provides insights into prenatal and early diagnosis of JS and expands the variation spectrum of C5orf42 gene. PMID: 29955609 [PubMed - in process]

https://www.ncbi.nlm.nih.gov/pubmed/29955609?dopt=Abstract

Source: Biomed Res - June 30, 2018 Category: Research Authors: Xiang J, Zhang L, Jiang W, Zhang Q, Wang T, Li H, Li H Tags: Biomed Res Int Source Type: research