Natalia Kalinchenko
2PUBLICATIONS
9CO-AUTHORS
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Publications (2)
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|Jul 01, 2022
A Founder Mutation in the POMC 5'-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA.Iuliia Viakhireva, Natalia Kalinchenko, Evgeny Vasilyev
|Mar 24, 2020
[Somatic mutations in the androgen receptor gene as the cause of androgen insensitivity syndrome].N Y Kalinchenko, A A Kolodkina, V M Petrov
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Frequent Collaborators
2 joint publications
Evgeny Vasilyev
2 joint publications
Anatoly Tiulpakov
1 joint publications
A A Kolodkina
1 joint publications
V M Petrov
1 joint publications
Iuliia Viakhireva
1 joint publications
Alexandra Filatova
1 joint publications
Andrey Marakhonov
1 joint publications
Petr M Rubtsov
1 joint publications
Mikhail Skoblov
