Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing

By Abuzenadah Adel   Zaher Galila   Dallol Ashraf   Damanhouri Ghazi   Chaudhary Adeel   Al-Sayes Faten   Gari Mamdooh   AlZahrani Mofareh   Hindawi Salwa   Al-Qahtani Mohammed  

Journal of Thrombosis and Thrombolysis, Vol. 36, Iss. 4, 2013-11 ,pp. : 501-506

Springer Publishing Company

Access to resources Recommend Favorite

From Whole Exome Sequencing to Patient‐Specific Therapy: Another Example of How Basic Research Pays Off in Patient Care

By  

JOURNAL OF THE AMERICAN HEART ASSOCIATION, Vol. 4, Iss. 5, 2015-05 ,pp. : n/a-n/a

John Wiley & Sons Inc

Access to resources Recommend Favorite

Genotyping using whole-genome sequencing is a realistic alternative to surveillance based on phenotypic antimicrobial susceptibility testing

By Zankari Ea   Hasman Henrik   Kaas Rolf Sommer   Seyfarth Anne Mette   Agersø Yvonne   Lund Ole   Larsen Mette Voldby   Aarestrup Frank M.  

Journal of Antimicrobial Chemotherapy, Vol. 68, Iss. 4, 2013-04 ,pp. : 771-777

Oxford University Press

Access to resources Recommend Favorite

Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients

By Tanskanen Tomas  

Scandinavian Journal of Gastroenterology, Vol. 48, Iss. 6, 2013-06 ,pp. : 672-678

Informa Healthcare

Access to resources Recommend Favorite

Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy

By  

JOURNAL OF THE AMERICAN HEART ASSOCIATION, Vol. 4, Iss. 12, 2015-12 ,pp. : n/a-n/a

John Wiley & Sons Inc

Access to resources Recommend Favorite