Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism
Küçük Resim Yok
Tarih
2018
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Nature Publishing Group
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
[Abstract Not Available]
Açıklama
Anahtar Kelimeler
Congenital Hypothyroidism, Genetic Test, Diagnosis
Kaynak
50th European-Society-of-Human-Genetics (ESHG) Conference
WoS Q Değeri
Q2
Scopus Q Değeri
Cilt
26
Sayı
Supplement: S
Künye
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.
