Natalia Bałdyga

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 6

Top Topics

High Throughput Sequencing

Autism Spectrum Disorder

Top Venues

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Dominika Oziębło, Natalia Bałdyga, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
Searching for the Molecular Basis of Partial Deafness. International journal of molecular sciences 23 (11) (2022)
Dominika Oziębło, Sang Yeon Lee, Marcin Ludwik Leja, Anna Sarosiak, Natalia Bałdyga, Henryk Skarzynski, Yehree Kim, Jin-Hee Han, Hyo Soon Yoo, Min-Hyun Park, Byung Yoon Choi, Monika Ołdak
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss. Human genetics 141 (3-4) (2022)