Funder
U.S. Department of Health & Human Services | NIH | National Institute of Mental Health
U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute
U.S. Department of Health & Human Services | NIH | U.S. National Library of Medicine
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference26 articles.
1. Nguengang Wakap, S. et al. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database. Eur. J. Hum. Genet. 28, 165–173 (2020).
2. Ferreira, C. R. The burden of rare diseases. Am. J. Med. Genet. A 179, 885–892 (2019).
3. Rosenthal, E. T., Biesecker, L. G. & Biesecker, B. B. Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes. Am. J. Med. Genet. 103, 106–114 (2001).
4. About Rare Diseases (Orphanet, accessed June 2020); https://www.orpha.net/consor/cgi-bin/Education_AboutRareDiseases.php?lng=EN
5. About Rare Diseases (EURORDIS Rare Diseases Europe, accessed June 2020); https://www.eurordis.org/about-rare-diseases
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