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Natalia Kalinchenko

2PUBLICATIONS

9CO-AUTHORS

Medical infection agents (incl. prions)Developmental genetics (incl. sex determination)

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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

Pageof 1

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

Frequent Collaborators

2 joint publications

Evgeny Vasilyev

2 joint publications

Anatoly Tiulpakov

1 joint publications

A A Kolodkina

1 joint publications

V M Petrov

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