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

McDermott, Helen
; 
Garikapati, Vidya
; 
Baptista, JĂșlia
; 
Gowda, Harsha
; 
Naik, Swati
Abstract
No abstract available
MIDER Authors
Garikapati, Vidya
Gowda, Harsha
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Date
2022-04-01
Type
Article
Subject
Genetics
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UHB Neo-Natal
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Citation
McDermott H, Garikapati V, Baptista J, Gowda H, Naik S. X-linked Ohdo syndrome due to a novel MED12 variant detected by Rapid Exome Sequencing. Clin Dysmorphol. 2022 Apr 1;31(2):101-105. doi: 10.1097/MCD.0000000000000412
Journal / Source Title
Clinical Dysmorphology
DOI
10.1097/MCD.0000000000000412
URI
http://hdl.handle.net/20.500.14200/6059
PMID
35102032
Publisher
Lippincott Williams & Wilkins
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