Identification of modifier genes underlying intra-familial phenotypic variability in zebrafish OI models using whole exome sequencing (WES) and linkage analysis
Main Authors: | Tamara Jarayseh, Adelbert De Clercq, Mauro Milazzo, Andy Willaert, Paul Coucke |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2021-04-01
|
Series: | Bone Reports |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2352187221003065 |
Similar Items
-
Identification of skeletal deformities towards deep phenotyping of zebrafish (Danio rerio) connective tissue disease models
by: Caitlin Debaene, et al.
Published: (2021-04-01) -
Parents’ Perspectives: Child’s Whole Exome Sequencing (WES) Research Results of Uncertain Significance
by: Tran, Grace
Published: (2014) -
Whole exome sequencing (WES) of methotrexate response/adverse event profile in rheumatoid arthritis patients
by: Lobna Abdel Salam, et al.
Published: (2021-10-01) -
Data Interoperability of Whole Exome Sequencing (WES) Based Mutational Burden Estimates from Different Laboratories
by: Ping Qiu, et al.
Published: (2016-04-01) -
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
by: Gordon K C Leung, et al.
Published: (2018-10-01)