ESHG: Tuesday, June 11

Tuesday, June 11, 2013
09.00 - 10.30	Plenary Session PL3: Large Scale Cohorts Studies to Identify Novel Highly Penetrant Genetic Disease Causing Variants
	PL3.1 Deciphering Developmental Disorders Project, Matt Hurles, United Kingdom PL3.2 Duke Fetal and Neonatal Cohort Study, Nicholas Katsanis, United States PL3.3 Ethical implications of Whole Genome Sequencing in medicine, Jane Kaye, United Kingdom

10.30 - 11.00	Coffee Break, Free Poster Viewing, Exhibition

11.00 - 12.30	Concurrent Sessions C15 - C20
	C15. NGS-based diagnostics C16. Developmental syndromes C17. Basic mechanisms in cytogenetics and molecular genetics C18. Big GWAS C19. Internal organs and endocrinology: Gene identification and function C20. Neurodevelopmental and neuropsychiatric disorders View details of concurrent sessions

12.30 - 13.30	Lunch, Exhibition, Poster Removal

13.30 - 14.15	Plenary Session PL4
	PL4.1 Mendel Lecture: Rett syndrome and MECP2 Disorders: From the Clinic to Genes and Neurobiology, Huda Zoghbi, United States

14.15 - 15.45	Plenary Session PL5
	PL5.1 ESHG Award Lecture, Felix Mitelman, Sweden ESHG Education Award EJHG Nature Awards Young Investigator & Poster Awards Closing

The European Society
of Human Genetics