Xia Wang
6PUBLICATIONS
30CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (6)
Sort by Publication Date:
|Jul 10, 2020
The expanding clinical phenotype of germline ABL1-associated congenital heart defects and skeletal malformations syndrome.Chun-An Chen, Emeline Crutcher, Harinder Gill
|Oct 04, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.Ash Zawerton, Cyril Mignot, Ashley Sigafoos
|Oct 24, 2018
Phenotypic expansion in DDX3X - a common cause of intellectual disability in females.Xia Wang, Jennifer E Posey, Jill A Rosenfeld
|Jan 27, 2017
The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencing.Yanming Feng, Xiaoyan Ge, Linyan Meng
|Oct 28, 2016
Retinal Diseases Caused by Mutations in Genes Not Specifically Associated with the Clinical Diagnosis.Xia Wang, Yanming Feng, Jianli Li
|Dec 04, 2015
Molecular diagnostic experience of whole-exome sequencing in adult patients.Jennifer E Posey, Jill A Rosenfeld, Regis A James
Pageof 1
Frequent Collaborators
3 joint publications
Jill A Rosenfeld
1 joint publications
Jennifer E Posey
1 joint publications
Shweta Dhar
1 joint publications
Jennifer Scull
1 joint publications
Jianli Li
1 joint publications
Tao Zhang
1 joint publications
Yue Wang
1 joint publications
Fangyuan Li
1 joint publications
Eric S Schmitt
1 joint publications
Yaping Yang
