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

Access

info:eu-repo/semantics/closedAccess

Date

2018

Author

Cangül, Hakan
Özel, Mavi Deniz
Genç, Nimetullah Mete
Kardelen Al, Aslı Derya
Darendeliler, Feyza

Metadata

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Citation

Cangül, H., Özel, M. D., Genç, N. M., Kardelen Al, A. D. ve Darendeliler, F. (2018). Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism. 50th European-Society-of-Human-Genetics (ESHG) Conference içinde (198-198. ss.). Copenhagen, Denmark, May 27-30, 2017.

Abstract

...

WoS Q Kategorisi

Q2

Source

50th European-Society-of-Human-Genetics (ESHG) Conference

Volume

26

Issue

Supplement: S

URI

https://hdl.handle.net/20.500.12511/6229

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