IdézéskapcsolatPoulsen L et al. X-linked recessive Menkes disease: Identification of partial gene deletions in affected males. (2002) CLINICAL GENETICS 0009-9163 1399-0004 62 6 449-457

Közlemény:
Bachrati CZ. Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families. (1998) ANNALS OF HUMAN GENETICS 0003-4800 1469-1809 62 6 511-520
Kapcsolódó cikk:
Poulsen L et al. X-linked recessive Menkes disease: Identification of partial gene deletions in affected males. (2002) CLINICAL GENETICS 0009-9163 1399-0004 62 6 449-457
Független: Igen
2020-11-30 21:49