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М. Саввина Т.
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Estimation of the heterozygote carrier frequency of frequent hereditary diseases in the Yakuts using oligonucleotide microarray
by
M. Savvina T.
,
N. Maksimova R.
,
A. Sukhomyasova L.
,
М
.
Саввина
Т
.
,
Н. Максимова Р.
,
А. Сухомясова Л.
Published in
Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
(2020)
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Related Subjects
3-M syndrome
3-М синдром
DNA-microarray
SOPH syndrome
SOPH-синдром
Yakuts
diagnostics
heterozygous carriage
inherited diseases
methaemoglobinaemia type 1
nonsyndromic hearing loss and deafness (DFNB1) type 1A
tyrosinemia type 1
биологический микрочип
гетерозиготное носительство
метгемоглобинемия 1 типа
наследственные заболевания
несиндромальная глухота 1 типа
тирозинемия 1 типа
якуты
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