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Dive into the research topics of 'Complex phenotype of dyskeratosis congenita and mood dysregulation with novel homozygous RTEL1 and TPH1 variants'. Together they form a unique fingerprint.- Sort by
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Rachel A. Ungar, Neelam Giri, Maryland Pao, Payal P. Khincha, Weiyin Zhou, Blanche P. Alter, Sharon A. Savage
Research output: Contribution to journal › Article › peer-review