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  5. Chromosome 21- uniparental disomy...

Chromosome 21- uniparental disomy of

December 31, 2014

News

  • Dicerna Announces Results for PHYOX™4, Single-Dose Study of Nedosira
  • NoviSystems Launches Fusion Analytics for Data-Driven Decision Making
  • Intellia Therapeutics Presents Preclinical Data Demonstrating Advancem
  • ENose Identifies Early Responders to Immunotherapy Among Non-Small Cel
  • Active Biotech and NeoTX today announce that the first patient has bee
More News

Treatment

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

Clinical Trial

  • Assessment of the Endovascular Aortic Aneurysm Repair’s (EVAR) M
  • CtDNA-MRD Based Adjuvant Targeted Therapy for EGFR Positive Stage I Lu
  • Percutaneous Coronary Intervention Before Transcatheter Aortic Valve I
  • Study of the Efficacy and Safety of Parsaclisib in Participants With P
  • High Medium-chain Triglyceride Nutritional Support in Infants With Bil
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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