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  5. Chromosome 21- uniparental disomy...

Chromosome 21- uniparental disomy of

December 31, 2014

News

  • Tonix Pharmaceuticals Announces Presentation at the Rare Disease Innov
  • What’s Next for Rare Disease Advocates?
  • Young patient powers past her disease to follow her dream
  • Biogen Appoints Chuck Triano as Head of Investor Relations
  • SeqOne Genomics Appoints HervĂ© Pouzoullic as Chief Commercial Officer
More News

Treatment

  • Flunarizine hydrochloride
  • Everolimus
  • Eribulin mesylate
  • Dexamethasone phosphate
  • Dantrolene sodium
More Treatment

Clinical Trial

  • A Study of Tumor-Treating Fields (TTFields) in People With Lung Adenoc
  • The Effects of Baduanjin Qigong Exercise on Ankylosing Spondylitis: A
  • Efficacy and Safety of BNP105 in the Treatment of Recurrent Aphthous S
  • An Early Clinical Trial to Evaluate VGN-R09b for Treatment of Aromatic
  • Role of Liquid Biopsies in HPV-associated Cancer Treatment Monitoring
More Clinical Trial

Access Program

  • Jonsson Comprehensive Cancer Center – Progressive Metastatic Cas
  • Massachusetts General Hospital – Healthy Naturally Cycling Women
  • Kite, A Gilead Company – Relapsed/Refractory Transformed Follicu
  • Kite, A Gilead Company – Relapsed/Refractory Primary Mediastinal
  • Kite, A Gilead Company – Relapsed/Refractory High-Grade B-Cell L
More Access Program

Disease

  • Neonatal alloimmune thrombocytopenia
  • Ubiquitin Disorder
  • Pseudo-Zellweger syndrome
  • Pseudoxanthoma elasticum- dominant form
  • Pseudoxanthoma elasticum- recessive form
More Disease

Research

  • Diagnostic Efficacy of Digital Dermoscopy and Clinical Findings in Thi
  • Differences in Characteristics and Outcomes Between Asian and Non-Asia
  • Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gi
  • Fetal akinesia deformation sequence due to a congenital disorder of gl
  • One case of torsades de pointes with Aase’s syndrome induced by
More Research

Network

  • Cures Within Reach
  • NGLY1.org
  • The Twin to Twin Transfusion Syndrome Foundation
  • Fetal Health Foundation
  • Plus One Foundation
More Network
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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