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Kostrzewa, Grazyna
62
results:
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Format
Online (62)
Mediatypes
Articles (Online) (36)
OpenAccess-fulltext (26)
Sorted by: Relevance
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1
Postzygotic mosaicism of a novel PTPN11 mutation in monozyg..:
Rydzanicz, Małgorzata
;
Glinkowski, Wojciech
;
Walczak, Anna
...
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1482-1487 , 2022
Link:
https://doi.org/10.1002/..
?
2
Clinical Presentation of Left Ventricular Noncompaction Car..:
Paszkowska, Agata
;
Piekutowska-Abramczuk, Dorota
;
Ciara, Elżbieta
...
Genes. 13 (2022) 3 - p. 477 , 2022
Link:
https://doi.org/10.3390/..
?
3
A recurrent de novo variant supports KCNC2 involvement in t..:
Rydzanicz, Małgorzata
;
Zwoliński, Piotr
;
Gasperowicz, Piotr
...
American Journal of Medical Genetics Part A. 185 (2021) 11 - p. 3384-3389 , 2021
Link:
https://doi.org/10.1002/..
?
4
Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Jo..:
Stembalska, Agnieszka
;
Rydzanicz, Małgorzata
;
Pollak, Agnieszka
...
Genes. 12 (2021) 7 - p. 1078 , 2021
Link:
https://doi.org/10.3390/..
?
5
Variable degree of mosaicism for tetrasomy 18p in phenotypi..:
Rydzanicz, Małgorzata
;
Olszewski, Pawel
;
Kedra, Darek
...
Molecular Genetics & Genomic Medicine. 9 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1002/..
?
6
Analysis of De Novo Mutations in Sporadic Cardiomyopathies ..:
Franaszczyk, Maria
;
Truszkowska, Grazyna
;
Chmielewski, Przemyslaw
...
Journal of Clinical Medicine. 9 (2020) 2 - p. 370 , 2020
Link:
https://doi.org/10.3390/..
?
7
Neurodevelopmental disorder associated with IRF2BPL gene mu..:
Skorvanek, Matej
;
Dusek, Petr
;
Rydzanicz, Malgorzata
...
Parkinsonism & Related Disorders. 62 (2019) - p. 239-241 , 2019
Link:
https://doi.org/10.1016/..
?
8
Novel COL12A1 variant as a cause of mild familial extracell..:
Jezela‐Stanek, Aleksandra
;
Walczak, Anna
;
Łaźniewski, Michał
...
Clinical Genetics. 95 (2019) 6 - p. 736-738 , 2019
Link:
https://doi.org/10.1111/..
?
9
Novel de novo mutation affecting two adjacent aminoacids in..:
Smigiel, Robert
;
Biernacka, Anna
;
Biela, Mateusz
...
Journal of Human Genetics. 63 (2018) 4 - p. 517-520 , 2018
Link:
https://doi.org/10.1038/..
?
10
Novel calcineurin A (PPP3CA) variant associated with epilep..:
Rydzanicz, Małgorzata
;
Wachowska, Małgorzata
;
Cook, Erik C.
...
European Journal of Human Genetics. 27 (2018) 1 - p. 61-69 , 2018
Link:
https://doi.org/10.1038/..
?
11
OXTR polymorphism in depression and completed suicide—A stu..:
Wasilewska, Krystyna
;
Pawlak, Aleksandra
;
Kostrzewa, Grażyna
...
Psychoneuroendocrinology. 77 (2017) - p. 84-89 , 2017
Link:
https://doi.org/10.1016/..
?
12
Mild Zellweger syndrome due to a novel PEX6 mutation: corre..:
Rydzanicz, Małgorzata
;
Stradomska, Teresa Joanna
;
Jurkiewicz, Elżbieta
...
Journal of Applied Genetics. 58 (2017) 4 - p. 475-480 , 2017
Link:
https://doi.org/10.1007/..
?
13
Intra- and inter-population analysis of haplotype diversity..:
Spólnicka, Magdalena
;
Dąbrowska, Joanna
;
Szabłowska-Gnap, Emilia
...
Forensic Science International: Genetics. 28 (2017) - p. e22-e25 , 2017
Link:
https://doi.org/10.1016/..
?
14
Haplotype dependent association of rs7927894 (11q13.5) with..:
Ponińska, Joanna Kinga
;
Samoliński, Bolesław
;
Tomaszewska, Aneta
...
PLOS ONE. 12 (2017) 9 - p. e0183922 , 2017
Link:
https://doi.org/10.1371/..
?
15
Further evidence for GRIN2B mutation as the cause of severe..:
Smigiel, Robert
;
Kostrzewa, Grazyna
;
Kosinska, Joanna
...
American Journal of Medical Genetics Part A. 170 (2016) 12 - p. 3265-3270 , 2016
Link:
https://doi.org/10.1002/..
1-15