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Search Results - Bartnik‐Glaska, Magdalena
Search Results - Bartnik‐Glaska, Magdalena
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Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss
by
Kowalczyk, Katarzyna
,
Smyk, Marta
,
Bartnik-Głaska, Magdalena
,
Plaskota, Izabela
,
Wiśniowiecka-Kowalnik, Barbara
,
Bernaciak, Joanna
,
Chojnacka, Marta
,
Paczkowska, Magdalena
,
Niemiec, Magdalena
,
Dutkiewicz, Daria
,
Kozar, Agata
,
Magdziak, Róża
,
Krawczyk, Wojciech
,
Pietras, Grzegorz
,
Michalak, Elżbieta
,
Klepacka, Teresa
,
Obersztyn, Ewa
,
Bal, Jerzy
,
Nowakowska, Beata Anna
Published in
Journal of assisted reproduction and genetics
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A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC)
by
Domaradzka, Justyna
,
Deperas, Marta
,
Obersztyn, Ewa
,
Kucińska-Chahwan, Anna
,
Brison, Nathalie
,
Van Den Bogaert, Kris
,
Roszkowski, Tomasz
,
Kędzior, Marta
,
Bartnik-Głaska, Magdalena
,
Łuszczek, Alicja
,
Jakubów-Durska, Krystyna
,
Vermeesch, Joris Robert
,
Nowakowska, Beata Anna
Published in
Molecular cytogenetics
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Diagnostic implications of genetic copy number variation in epilepsy plus
by
Coppola, Antonietta
,
Cellini, Elena
,
Stamberger, Hannah
,
Saarentaus, Elmo
,
Cetica, Valentina
,
Lal, Dennis
,
Djémié, Tania
,
Bartnik‐Glaska, Magdalena
,
Ceulemans, Berten
,
Helen Cross, J.
,
Deconinck, Tine
,
Masi, Salvatore De
,
Dorn, Thomas
,
Guerrini, Renzo
,
Hoffman‐Zacharska, Dorotha
,
Kooy, Frank
,
Lagae, Lieven
,
Lench, Nicholas
,
Lemke, Johannes R.
,
Lucenteforte, Ersilia
,
Madia, Francesca
,
Mefford, Heather C.
,
Morrogh, Deborah
,
Nuernberg, Peter
,
Palotie, Aarno
,
Schoonjans, An‐Sofie
,
Striano, Pasquale
,
Szczepanik, Elzbieta
,
Tostevin, Anna
,
Vermeesch, Joris R.
,
Van Esch, Hilde
,
Van Paesschen, Wim
,
Waters, Jonathan J
,
Weckhuysen, Sarah
,
Zara, Federico
,
De Jonghe, Peter
,
Sisodiya, Sanjay M.
,
Marini, Carla
,
Lehesjioki, Anna‐Elina
,
Craiu, Dana
,
Talvik, Tiina
,
Caglayan, Hande
,
Serratosa, Jose
,
Sterbova, Katalin
,
Møller, Rikke S.
,
Hjalgrim, Helle
,
Lerche, Holger
,
Weber, Yvonne
,
Helbig, Ingo
,
Spiczak, Sarah
,
Barba, Carmen
,
Bogaerts, Anneleen
,
Boni, Antonella
,
Galizia, Elisabeth Caruana
,
Chiari, Sara
,
Gacomo, Gianpiero
,
Ferrari, Annarita
,
Guarducci, Silvia
,
Giglio, Sabrina
,
Holmgren, Philip
,
Leu, Costin
,
Melani, Federico
,
Novara, Francesca
,
Pantaleo, Marilena
,
Peeters, Elke
,
Pisano, Tiziana
,
Rosati, Anna
,
Sander, Josemir
,
Schoeler, Natasha
,
Stankiewicz, Pawel
,
Striano, Salvatore
,
Suls, Arvid
,
Traverso, Monica
,
Vandeweyer, Geert
,
Dijck, Anke
,
Zuffardi, Orsetta
Published in
Epilepsia (Copenhagen)
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Cytogenomic features of Richter transformation
by
Woroniecka, Renata
,
Rymkiewicz, Grzegorz
,
Bystydzienski, Zbigniew
,
Pienkowska-Grela, Barbara
,
Rygier, Jolanta
,
Malawska, Natalia
,
Wojtkowska, Katarzyna
,
Goral, Nikolina
,
Blachnio, Katarzyna
,
Chmielewski, Marcin
,
Bartnik-Glaska, Magdalena
,
Grygalewicz, Beata
Published in
Molecular cytogenetics
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How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review
by
Wielgos, Miroslaw
,
Kosinski, Przemyslaw
,
Jedrzejak, Piotr
,
Krajewska-Walasek, Małgorzata
,
Bartnik-Glaska, Magdalena
,
Nowakowska, Beata
,
Jezela-Stanek, Aleksandra
Published in
Taiwanese journal of obstetrics & gynecology
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Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities
by
Kowalczyk, Katarzyna
,
Bartnik-Głaska, Magdalena
,
Smyk, Marta
,
Plaskota, Izabela
,
Bernaciak, Joanna
,
Kędzior, Marta
,
Wiśniowiecka-Kowalnik, Barbara
,
Jakubów-Durska, Krystyna
,
Braun-Walicka, Natalia
,
Barczyk, Artur
,
Geremek, Maciej
,
Castañeda, Jennifer
,
Kutkowska-Kaźmierczak, Anna
,
Własienko, Paweł
,
Dębska, Marzena
,
Kucińska-Chahwan, Anna
,
Roszkowski, Tomasz
,
Kozłowski, Szymon
,
Mikulska, Boyana
,
Issat, Tadeusz
,
Obersztyn, Ewa
,
Nowakowska, Beata Anna
Published in
Genes
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Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome
by
Smyk, Marta
,
Geremek, Maciej
,
Ziemkiewicz, Kamila
,
Gambin, Tomasz
,
Kutkowska-Kaźmierczak, Anna
,
Kowalczyk, Katarzyna
,
Plaskota, Izabela
,
Wiśniowiecka-Kowalnik, Barbara
,
Bartnik-Głaska, Magdalena
,
Niemiec, Magdalena
,
Grad, Dominika
,
Piotrowicz, Małgorzata
,
Gieruszczak-Białek, Dorota
,
Pietrzyk, Aleksandra
,
Crowley, T Blaine
,
Giunta, Victoria
,
McGinn, Daniel E
,
Zackai, Elaine H
,
Tran, Oanh
,
Emanuel, Beverly S
,
McDonald-McGinn, Donna M
,
Nowakowska, Beata A
Published in
Genes
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Multiple occurrence of psychomotor retardation and recurrent miscarriages in a family with a submicroscopic reciprocal translocation t(7;17)(p22;p13.2)
by
Pasińska, Magdalena
,
Łazarczyk, Ewelina
,
Jułga, Katarzyna
,
Bartnik-Głaska, Magdalena
,
Nowakowska, Beata
,
Haus, Olga
Published in
BMC medical genomics
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Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15
by
Pesz, Karolina
,
Pienkowski, Victor Murcia
,
Pollak, Agnieszka
,
Gasperowicz, Piotr
,
Sykulski, Maciej
,
Kosińska, Joanna
,
Kiszko, Magdalena
,
Krzykwa, Bogusława
,
Bartnik-Głaska, Magdalena
,
Nowakowska, Beata
,
Rydzanicz, Małgorzata
,
Sasiadek, Maria Małgorzata
,
Płoski, Rafał
Published in
European journal of medical genetics
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Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies
by
Kowalczyk, Katarzyna
,
Bartnik-Głaska, Magdalena
,
Smyk, Marta
,
Plaskota, Izabela
,
Bernaciak, Joanna
,
Kędzior, Marta
,
Wiśniowiecka-Kowalnik, Barbara
,
Deperas, Marta
,
Domaradzka, Justyna
,
Łuszczek, Alicja
,
Dutkiewicz, Daria
,
Kozar, Agata
,
Grad, Dominika
,
Niemiec, Magdalena
,
Ziemkiewicz, Kamila
,
Magdziak, Róża
,
Braun-Walicka, Natalia
,
Barczyk, Artur
,
Geremek, Maciej
,
Castañeda, Jennifer
,
Kutkowska-Kaźmierczak, Anna
,
Własienko, Paweł
,
Jakubów-Durska, Krystyna
,
Dębska, Marzena
,
Kucińska-Chahwan, Anna
,
Kozłowski, Szymon
,
Mikulska, Boyana
,
Issat, Tadeusz
,
Roszkowski, Tomasz
,
Nawara-Baran, Agnieszka
,
Runge, Agata
,
Jakubiuk-Tomaszuk, Anna
,
Kruczek, Anna
,
Kostyk, Ewa
,
Pietras, Grzegorz
,
Limon, Janusz
,
Zwoliński, Jerzy
,
Ochman, Karolina
,
Szajner, Tomasz
,
Węgrzyn, Piotr
,
Wielgoś, Mirosław
,
Sąsiadek, Maria
,
Obersztyn, Ewa
,
Nowakowska, Beata Anna
Published in
Genes
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The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (P.GLN1981)
by
Dawidziuk, Mateusz
,
Kutkowska-Kaźmierczak, Anna
,
Gawliński, Paweł
,
Wiszniewski, Wojciech
,
Gos, Monika
,
Stawiński, Piotr
,
Rydzanicz, Małgorzata
,
Kosińska, Joanna
,
Własienko, Paweł
,
Malinowska Kordowska, Olga
,
Bartnik-Głaska, Magdalena
,
Bernaciak, Joanna
,
Szczałuba, Krzysztof
,
Bekiesińska-Figatowska, Monika
,
Płoski, Rafał
,
Bal, Jerzy
,
Olimpia Rzońca-Niewczas, Sylwia
Published in
Journal of Mother and Child
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