Magdalena Pelc

Minimal clinical findings in a patient with 15qter microdeletion syndrome: Delineation of the associated phenotype

Aleksandra Jezela‐Stanek, Marzena Kucharczyk, Magdalena Pelc et al. · American Journal of Medical Genetics Part A · 2012 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Diagnostic and therapeutic value of human serpin family proteins

Sabina Janciauskiene, Urszula Lechowicz, Magdalena Pelc et al. · Biomedicine & Pharmacotherapy · 2024 · 34 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +10

Spectrum of JAG1 gene mutations in Polish patients with Alagille syndrome

Dorota Jurkiewicz, Dorota Gliwicz, Elżbieta Ciara et al. · Journal of Applied Genetics · 2014 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Phenotype expansion and development in Kosaki overgrowth syndrome

Paweł Gawliński, Magdalena Pelc, Elżbieta Ciara et al. · Clinical Genetics · 2017 · 28 citations

Medicine, Molecular Genetics, Pathobiology +14

Cryptic X; Autosome Translocation in a Boy—Delineation of the Phenotype

Aleksandra Jezela‐Stanek, Elżbieta Ciara, Marzena Juszczak et al. · Pediatric Neurology · 2011 · 12 citations

Life Sciences, Genetics, Molecular Genetics +12