Hasil Pencarian - Marzena Kucharczyk
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1
Oculocutaneous albinism in a patient with 17p13.2-pter duplication - a review on the molecular syndromology of 17p13 duplication oleh Marzena Kucharczyk, Aleksandra Jezela-Stanek, Dorota Gieruszczak-Bialek, Monika Kugaudo, Agata Cieslikowska, Magdalena Pelc, Malgorzata Krajewska-Walasek
Diterbitkan 2015-06-01Dapatkan teks lengkap
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2
DNA Oxidative Cleavage Induced by the Novel Peptide Derivatives of 3-(quinoxalin-6-yl)alanine in Combination with Cu(II) or Fe(II) Ions oleh Wojciech Szczepanik, Marzena Kucharczyk-Klamińska, Piotr Stefanowicz, Anna Staszewska, Zbigniew Szewczuk, Jacek Skała, Andrzej Mysiak, Małgorzata Jeżowska-Bojczuk
Diterbitkan 2009-01-01Dapatkan teks lengkap
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3
The phenotype‐driven computational analysis yields clinical diagnosis for patients with atypical manifestations of known intellectual disability syndromes oleh Aleksandra Jezela‐Stanek, Elżbieta Ciara, Dorota Jurkiewicz, Marzena Kucharczyk, Maria Jędrzejowska, Krystyna H. Chrzanowska, Małgorzata Krajewska‐Walasek, Tomasz Żemojtel
Diterbitkan 2020-09-01Dapatkan teks lengkap
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4
Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant oleh Aleksandra Jezela-Stanek, Marzena Kucharczyk, Katarzyna Falana, Dorota Jurkiewicz, Marlena Mlynek, Dorota Wicher, Malgorzata Rydzanicz, Monika Kugaudo, Agata Cieslikowska, Elzbieta Ciara, Rafal Ploski, Malgorzata Krajewska-Walasek
Diterbitkan 2016-03-01Dapatkan teks lengkap
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