A rare hereditary connective tissue disease associated with the TGF-? signalling pathway:a case study of Loeys-Dietz syndrome type 1
Küçük Resim Yok
Tarih
2019
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Nature Publishing Group
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
[Abstract Not Availabe]
Açıklama
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY
Anahtar Kelimeler
[Keyword Not Available]
Kaynak
European Journal Of Human Genetics
WoS Q Değeri
Q2
Scopus Q Değeri
Q1
Cilt
27