Anna Szoszkiewicz

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 7

Top Topics

Bone Mineral Density

Postmenopausal Women

Top Venues

Journal of applied genetics

Orphanet journal of rare diseases

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

Publications

Anna Szoszkiewicz, Ewelina M Olech, Aleksander Jamsheer
Molecular landscape of congenital vertebral malformations: recent discoveries and future directions. Orphanet journal of rare diseases 19 (1) (2024)
Anna Szoszkiewicz, Ewelina M Olech, Aleksander Jamsheer
Molecular landscape of congenital vertebral malformations: recent discoveries and future directions. Orphanet journal of rare diseases 19 (1) (2024)
Anna Szoszkiewicz, Ewelina M Olech, Aleksander Jamsheer
Molecular landscape of congenital vertebral malformations: recent discoveries and future directions. Orphanet journal of rare diseases 19 (1) (2024)
Magdalena Socha, Anna Szoszkiewicz, Dorota Simon, Aleksander Jamsheer
A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndrome. Journal of applied genetics (2022)
Magdalena Socha, Anna Szoszkiewicz, Dorota Simon, Aleksander Jamsheer
A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndrome. Journal of applied genetics 64 (1) (2022)
Magdalena Socha, Anna Szoszkiewicz, Dorota Simon, Aleksander Jamsheer
A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndrome. Journal of applied genetics 64 (1) (2022)
Magdalena Socha, Anna Szoszkiewicz, Dorota Simon, Aleksander Jamsheer
A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndrome. Journal of applied genetics 64 (1) (2022)