english türkçe
Yeni ve İyileştirilmiş Ürünler
Application Region Art.Nr.
Cystic Fibrosis CFTR 7q31.2 P091
Faciogenital dysplasia (FGDY), Aarskog-Scott syndrome FGD1 Xp11.21 P232
Familial lymphohistiocytosis (HLH) UNC13D 17q25.1, PRF1 10q22.1, STX11 6q24.2 P028
Haemolytic Anaemia, hereditary non-spherocytic PKLR 1q22 P203
Hypertrophic cardiomyopathy MYH7 14q11.2 P418
Leigh Syndrome X-chromosome P427
Mediterranean fever, familial (MEFV) MEFV 16p13.3 P094
Thiopurine S-methyltransferase (TPMT; S-adenosyl-L-methionine:thiopurine S-methyltransferase) TPMT 6p22, DPYD 1p22 P283
nondystrophic myotonias and primary periodic paralyses CACNA1S, SCN4A P397

Copyright © 2009 - 2018 İnvitrotek A.Ş. All Right Reserved by Invitrotek

Copyright © 2009 - 2018 İnvitrotek A.Ş. All Right Reserved by Invitrotek
Powered by EOS