Bożena Anna Marszałek-Kruk

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 8

Top Topics

Autism Spectrum Disorder

Top Venues

Children (Basel, Switzerland)

Human genome variation

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

Publications

Kulesa-Mrowiecka Małgorzata, Anna Lipowicz, Bożena Anna Marszałek-Kruk, Damian Kania, Wojciech Wolański, Andrzej P Myśliwiec, Krzysztof Dowgierd
Characteristics of Factors Influencing the Occurrence of Cleft Lip and/or Palate: A Case Analysis and Literature Review. Children (Basel, Switzerland) 11 (4) (2024)
Kulesa-Mrowiecka Małgorzata, Anna Lipowicz, Bożena Anna Marszałek-Kruk, Damian Kania, Wojciech Wolański, Andrzej P Myśliwiec, Krzysztof Dowgierd
Characteristics of Factors Influencing the Occurrence of Cleft Lip and/or Palate: A Case Analysis and Literature Review. Children (Basel, Switzerland) 11 (4) (2024)
Bożena Anna Marszałek-Kruk, Andrzej P Myśliwiec, Anna Lipowicz, Wojciech Wolański, Małgorzata Kulesa-Mrowiecka, Krzysztof Dowgierd
Children with Rare Nager Syndrome-Literature Review, Clinical and Physiotherapeutic Management. Genes 15 (1) (2023)
Bożena Anna Marszałek-Kruk, Andrzej P Myśliwiec, Anna Lipowicz, Wojciech Wolański, Małgorzata Kulesa-Mrowiecka, Krzysztof Dowgierd
Children with Rare Nager Syndrome-Literature Review, Clinical and Physiotherapeutic Management. Genes 15 (1) (2023)
Bożena Anna Marszałek-Kruk, Andrzej P Myśliwiec, Anna Lipowicz, Wojciech Wolański, Małgorzata Kulesa-Mrowiecka, Krzysztof Dowgierd
Children with Rare Nager Syndrome-Literature Review, Clinical and Physiotherapeutic Management. Genes 15 (1) (2023)
Bożena Anna Marszałek-Kruk, Andrzej P Myśliwiec, Anna Lipowicz, Wojciech Wolański, Małgorzata Kulesa-Mrowiecka, Krzysztof Dowgierd
Children with Rare Nager Syndrome-Literature Review, Clinical and Physiotherapeutic Management. Genes 15 (1) (2023)
Bożena Anna Marszałek-Kruk, Piotr Wójcicki
Identification of three novel TCOF1 mutations in patients with Treacher Collins Syndrome. Human genome variation 8 (1) (2021)
Bożena Anna Marszałek-Kruk, Piotr Wójcicki, Krzysztof Dowgierd, Smigiel Robert
Treacher Collins Syndrome: Genetics, Clinical Features and Management. Genes 12 (9) (2021)