Lukasz Kuszel

SMD Kozlowski type caused by p.Arg594His substitution in TRPV4 reveals abnormal ossification and notochordal remnants in discs and vertebrae.

P. Beighton, M. Czarny-Ratajczak, K. Kozłowski, 2017, European journal of medical genetics.

Severe neonatal spondylometaphyseal dysplasia in two siblings

K. Chrzanowska, L. Jakubowski, M. Czarny-Ratajczak, 2009, American journal of medical genetics. Part A.

Prevalence of Anti-SARS-CoV-2 Antibodies in Poznań, Poland, after the First Wave of the COVID-19 Pandemic

R. Kierzek, P. Zmora, L. Kuszel, 2021, medRxiv.

Homozygous microdeletion in the 11p13 region in the patient with isolated form of aniridia: New challenges in the genetic diagnostics of aniridia

A. Wawrocka, M. Krawczyński, B. Budny, 2021, American journal of medical genetics. Part A.

11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia

A. Wawrocka, M. Krawczyński, Lukasz Kuszel, 2013, Journal of Applied Genetics.

Osteoarthritis and telomere shortening

T. Trzeciak, M. Richter, M. Czarny-Ratajczak, 2014, Journal of Applied Genetics.

Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations

A. Latos-Bieleńska, A. Wawrocka, A. Wnuk, 2017, American journal of medical genetics. Part A.

A new form or a variant of SMD type A4

M. Czarny-Ratajczak, O. Hudakova, K. Kozłowski, 2012, Journal of Applied Genetics.