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ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison.
Barclay SF, Rand CM, Nguyen L, Wilson RJA, Wevrick R, Gibson WT, Bech-Hansen NT, Weese-Mayer DE. Barclay SF, et al. Among authors: wevrick r. Orphanet J Rare Dis. 2018 Jul 20;13(1):124. doi: 10.1186/s13023-018-0860-0. Orphanet J Rare Dis. 2018. PMID: 30029683 Free PMC article.
75 results