X-linked Ohdo syndrome due to a novel MED12 variant detected by Rapid Exome Sequencing

Authors

Helen McDermott, University Hospitals Birmingham NHS Foundation Trust
Vidya Garikapati, University Hospitals Birmingham NHS Foundation Trust
Júlia Baptista, Peninsula Medical School
Harsha Gowda, University Hospitals Birmingham NHS Foundation Trust
Swati Naik, Birmingham Women's and Children's NHS Foundation Trust

ORCID

• Júlia Baptista: 0000-0003-0915-5028

DOI

10.1097/mcd.0000000000000412

Publication Date

2022-01-01

Publication Title

Clinical Dysmorphology

Volume

31

Issue

2

ISSN

0962-8827

Embargo Period

2023-04-01

First Page

101

Last Page

105

Recommended Citation

McDermott, H., Garikapati, V., Baptista, J., Gowda, H., & Naik, S. (2022) 'X-linked Ohdo syndrome due to a novel MED12 variant detected by Rapid Exome Sequencing', Clinical Dysmorphology, 31(2), pp. 101-105. Available at: 10.1097/mcd.0000000000000412