Studying of genetic markers prevalence of congenital adrenal hyperplasia 21-hydroxylase deficiency in children of native small in numbers people of the Far North and general approaches to the modelling of hereditary pathology prevalence in children’s population
Abstract
In work data of the pilot project on studying of prevalence of deficiency 21-ОН genetic markers in populations of the Far North are presented. 463 DNA samples of children living in Republic Sakha (Yakutia) and Yamal-Nenets autonomous region are surveyed by method of polymerase chain reaction.
About the Authors
V. G. Chasnyk
Санкт-Петербургская гос. Педиатрическая мед. академия
Russian Federation
Russian Federation
S. J. Jakovleva
Консультативная поликлиника Педиатрического центра РБ №1-НЦМ
Russian Federation
Russian Federation
T. E. Burtseva
ЯНЦ КМП СО РАМН
Russian Federation
Russian Federation
M. I. New
больница Маунт Синай
United States
United States
E. V. Sinelnikova
СПбГПМА
Russian Federation
Russian Federation
S. L. Avrusin
СПбГПМА
Russian Federation
Russian Federation
V. P. Shadrin
Якутская детская гор. больница
Russian Federation
Russian Federation
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Review
For citations:
Chasnyk V.G., Jakovleva S.J., Burtseva T.E., New M.I., Sinelnikova E.V., Avrusin S.L., Shadrin V.P. Studying of genetic markers prevalence of congenital adrenal hyperplasia 21-hydroxylase deficiency in children of native small in numbers people of the Far North and general approaches to the modelling of hereditary pathology prevalence in children’s population. Yakut Medical Journal. 2009;(2):20-22. (In Russ.)
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