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 Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children Lijun Fan, Xiaoya Ren, Yanning Song, Chang Su, Junfen Fu and Chunxiu Gong Orphanet Journal of Rare Diseases 2019, 14:299 | Published on: 30 December 2019 Full Text | PDF REVIEW The evolving therapeutic landscape of genetic skeletal disorders Ataf Hussain Sabir and Trevor Cole Orphanet Journal of Rare Diseases 2019, 14:300 | Published on: 30 December 2019 Full Text | PDF

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