Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy by Jann Adriel Chua Sy, Jann Adriel Chua Sy, Poh Lin Tan, Poh Lin Tan, Jeremy Bingyuan Lin, Jeremy Bingyuan Lin, Stacey Kiat-Hong Tay, Stacey Kiat-Hong Tay, Hui-Lin Chin, Hui-Lin Chin

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