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Dive into the research topics of 'NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness'. Together they form a unique fingerprint.- Sort by
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Kerry K Brown, Fowzan S Alkuraya, Michael Matos, Richard L Robertson, Virginia E Kimonis, Cynthia C Morton
Research output: Contribution to journal › Article › peer-review