Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism | AVESİS

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Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism

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Cangul H., Ozel M., Genc N., Kardelen A. D., Darendeliler F.

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.198

Publication Type: Conference Paper / Summary Text
Volume: 26
City: Copenhagen
Country: Denmark
Page Numbers: pp.198
Istanbul University Affiliated: Yes