Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients Lili Yang, Qiong Zhou, Bo Ma, Shujiong Mao, Yanli Dai, Mingqiang Zhu and Chaochun Zou Orphanet Journal of Rare Diseases 2020, 15:24 | Published on: 21 January 2020 Full Text | PDF REVIEW A systematic review on the burden of illness in individuals with tuberous sclerosis complex (TSC) Johann Philipp Zöllner, David Neal Franz, Christoph Hertzberg, Rima Nabbout, Felix Rosenow, Matthias Sauter, Susanne Schubert-Bast, Adelheid Wiemer-Kruel and Adam Strzelczyk Orphanet Journal of Rare Diseases 2020, 15:23 | Published on: 21 January 2020 Full Text | PDF

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