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Article

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

Clinical dysmorphology - 1 Apr 2022

McDermott Helen, Garikapati Vidya, Baptista Júlia, Gowda Harsha, Naik Swati

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Share to Abnormalities, Multiple
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 35102032
DOI: 10.1097/MCD.0000000000000412

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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