"Whole‐exome sequencing identified compound heterozygous variants in ROR2 gene in a fetus with Robinow syndrome"

LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Autosomal recessive Robinow syndrome (ARRS) is a rare genetic disorder, which affects the development of multiple systems, particularly the bones. Click to show full abstract

Autosomal recessive Robinow syndrome (ARRS) is a rare genetic disorder, which affects the development of multiple systems, particularly the bones.

Keywords: exome sequencing; identified compound; whole exome; sequencing identified; robinow syndrome; compound heterozygous

Journal Title: Journal of Clinical Laboratory Analysis
Year Published: 2019

Link to full text (if available)

Share on Social Media: Sign Up to like & get
recommendations!
1

LAUSR

You are not signed in:

Sign Up!

Related content

More Information News Social Media Video Recommended