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 Quality of life of children with achondroplasia and their parents - a German cross-sectional study Stefanie Witt, Beate Kolb, Janika Bloemeke, Klaus Mohnike, Monika Bullinger and Julia Quitmann Orphanet Journal of Rare Diseases 2019, 14:194 | Published on: 9 August 2019 Full Text | PDF RESEARCH Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis M. Fernanda Rozas, Felipe Benavides, Luis León and Gabriela M. Repetto Orphanet Journal of Rare Diseases 2019, 14:195 | Published on: 9 August 2019 Full Text | PDF RESEARCH Natural history of patients with venous thromboembolism and hereditary hemorrhagic telangiectasia. Findings from the RIETE registry Antoni Riera-Mestre, José María Mora-Luján, Javier Trujillo-Santos, Jorge Del Toro, José Antonio Nieto, José María Pedrajas, Raquel López-Reyes, Silvia Soler, Aitor Ballaz, Pau Cerdà and Manel Monreal Orphanet Journal of Rare Diseases 2019, 14:196 | Published on: 9 August 2019 Full Text | PDF

Follow BMC on: . For further information or enquiries please use our contact page details. BMC respects your privacy and does not disclose, sell or rent your personal information to any non-affliated third parties with your consent. Privacy policy. BioMed Central Ltd The Campus, 4 Crinan Street, London, N1 9XW, United Kingdom

© 2019 BioMed Central Limited unless otherwise stated. Part of Springer Nature.