Discovery of Genetic Basis of Mendelian or Monogenic Heart, Lung, and Blood Disorders (X01)

קרןNational Heart, Lung, and Blood Institute/NIH
סוגIn Kind
תאריך אחרון15/07/2018
פקולטהLife Sciences, Medicine

The NHLBI invites applications to use the exome sequencing capacity of the Mendelian Disorders Genome Centers to carry out studies to investigate the genetic basis of Mendelian or monogenic disorders that significantly affect heart, lung, and blood (HLB) systems.


Funding: N/A (sequencing services)
Duration: 4 years


LOI (encouraged) due date: 20.9.15, 15.5.16, 15.5.17, 15.5.18
Full proposal due date: 20.10.15, 15.6.16, 15.6.17, 15.6.18​

קבצים מצורפים
עדכון אחרוןעדכון אחרון: 30/07/2015
אוניברסיטת תל-אביב, ת.ד. 39040, תל-אביב 6997801
UI/UX Basch_Interactive