Oligonucleotide microarray based method for simultaneous diagnostic of 3-M syndrome, SOPH syndrome, tyrosinemia type 1, methaemoglobinaemia type 1, nonsyndromic hearing loss and deafness (DFNB1)

M. T. Savvina; A. L. Sukhomyamova; P. I. Golikova; A. L. Danilova; N. R. Maksimova

For citations:

Savvina M.T., Sukhomyamova A.L., Golikova P.I., Danilova A.L., Maksimova N.R. Oligonucleotide microarray based method for simultaneous diagnostic of 3-M syndrome, SOPH syndrome, tyrosinemia type 1, methaemoglobinaemia type 1, nonsyndromic hearing loss and deafness (DFNB1). Medical Genetics. 2019;18(9):24-33. (In Russ.) https://doi.org/10.25557/2073-7998.2019.09.24-33

This work is licensed under a Creative Commons Attribution 4.0 License.

ISSN 2073-7998 (Print)

Username
Password
	Remember me
Not a user? Register with this site Forgot your password?

User

Medical Genetics

For citations:

Cookies policy