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“A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops.”: a case report
Panicos Shangaris, Alison Ho, Andreas Marnerides, Simi George, A Mudher, Shu Yau, Mattias Jansson, Jacqui Hoyle, Joo Wook Ahn, S Ellard, Melita Irving, Diana Wellesley, Dharmintra Pasupathy, Muriel Holder-Espinasse
Research output: Contribution to journal › Article › peer-review
2
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(Scopus)