toggle visibility Search & Display Options

Select All    Deselect All
List View
 |   | 
   print
  Author Title Year Publication (up) Volume Pages Links
Smith, John; Smith, Jane Some very captivating research 2017 details   openurl
Kueppers, F.; Sanders, C. State-of-the-art testing for alpha-1 antitrypsin deficiency 2017 Allergy and Asthma Proceedings 38 108-114 details   doi
Vershkov, D.; Benvenisty, N. Human pluripotent stem cells in modeling human disorders: the case of fragile X syndrome 2017 Regenerative Medicine 12 53-68 details   doi
Li, M.; Zhao, H.; Ananiev, G.E.; Musser, M.T.; Ness, K.H.; Maglaque, D.L.; Saha, K.; Bhattacharyya, A.; Zhao, X. Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells 2017 Stem Cells (Dayton, Ohio) 35 158-169 details   doi
Polex-Wolf, J.; Yeo, G.S.H.; O'Rahilly, S. Impaired prohormone processing: a grand unified theory for features of Prader-Willi syndrome? 2017 The Journal of Clinical Investigation 127 98-99 details   doi
Select All    Deselect All
List View
 |   | 
   print

Save Citations:
Export Records: