Sebastian Kwiatkowski
6PUBLICATIONS
71CO-AUTHORS
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Publications (6)
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|May 02, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion.Keng Ioi Vong, Sangmoon Lee, Kit Sing Au
|May 13, 2022
Prenatal diagnosis of acrania/exencephaly/anencephaly sequence (AEAS): additional structural and genetic anomalies.Julia Bijok, Sylwia Dąbkowska, Anna Kucińska-Chahwan
|Mar 22, 2022
Recommendations for prenatal diagnostics of the Polish Society of Gynaecologists and Obstetricians and the Polish Society of Human Genetics.Piotr Sieroszewski, Olga Haus, Mariusz Zimmer
|Jul 01, 2021
Extended genetic testing in fetuses with sonographic skeletal system abnormalities.A Kucińska-Chahwan, T Roszkowski, B Nowakowska
|Jan 15, 2021
Prenatal diagnosis of glutaric acidemia type 2 with the use of exome sequencing - an up-to-date review and new case report.Anna M Kucinska-Chahwan, Tomasz Roszkowski, Maciej Geremek
|Sep 03, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition.Marta Unolt, Molka Kammoun, Beata Nowakowska
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Frequent Collaborators
3 joint publications
Tomasz Roszkowski
3 joint publications
Maciej Geremek
3 joint publications
Julia Bijok
3 joint publications
Diana Massalska
2 joint publications
Anna M Kucinska-Chahwan
2 joint publications
Donna McDonald-McGinn
2 joint publications
Hanna Moczulska
2 joint publications
Elaine H Zackai
2 joint publications
T Blaine Crowley
1 joint publications
M Paczkowska
