MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome

por Bik-Multanowski, Miroslaw, Pietrzyk, Jacek J., Midro, Alina
Publicado en J Alzheimers Dis (2015)

Abilities of development support in children with genetic syndromes. Experiences from annual integrational meetings

por Midro, Alina T, Haus, Olga, Kobel-Buys, Krystyna, Wierzba, Jolanta, Zajączek, Stanisław
Publicado 2010

Complex balanced chromosomal translocation t(2;5;13) (p21;p15;q22) in a woman with four reproductive failures

por Lazarczyk, Ewelina, Drozniewska, Malgorzata, Pasinska, Magdalena, Stasiewicz-Jarocka, Beata, Midro, Alina T, Haus, Olga
Publicado en Mol Cytogenet (2014)

Chromosome (re)positioning in spermatozoa of fathers and sons – carriers of reciprocal chromosome translocation (RCT)

por Olszewska, Marta, Wiland, Ewa, Huleyuk, Nataliya, Fraczek, Monika, Midro, Alina T., Zastavna, Danuta, Kurpisz, Maciej
Publicado en BMC Med Genomics (2019)

Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations

por Šumanović-Glamuzina, Darinka, Lozić, Bernarda, Iwanowski, Piotr S., Zemunik, Tatijana, Bilinovac, Zeljka, Stasiewicz-Jarocka, Beata, Panasiuk, Barbara, Midro, Alina T.
Publicado en Mol Cytogenet (2017)

Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1

por Midro, Alina T., Zollino, Marcella, Wiland, Ewa, Panasiuk, Barbara, Iwanowski, Piotr S., Murdolo, Marina, Śmigiel, Robert, Sąsiadek, Maria, Pilch, Jacek, Kurpisz, Maciej
Publicado en J Assist Reprod Genet (2015)

Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male

por Wiland, Ewa, Olszewska, Marta, Georgiadis, Andrew, Huleyuk, Nataliya, Panasiuk, Barbara, Zastavna, Danuta, Yatsenko, Svetlana A, Jedrzejczak, Piotr, Midro, Alina T, Yatsenko, Alexander N, Kurpisz, Maciej
Publicado 2014

Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies

por Glinton, Kevin E., Hurst, Anna C. E., Bowling, Kevin M., Cristian, Ingrid, Haynes, Devon, Adstamongkonkul, Dusit, Schnappauf, Oskar, Beck, David B., Brewer, Carole, Parikh, Aditi Shah, Shinde, Deepali N., Donaldson, Alan, Brautbar, Ariel, Koene, Saskia, van Haeringen, Arie, Piton, Amélie, Capri, Yline, Furlan, Margherita, Gardella, Elena, Møller, Rikke Steensbjerre, van de Beek, Irma, Zuurbier, Linda, Lakeman, Phillis, Bayat, Allan, Martinez, Julian, Signer, Rebecca, Torring, Pernille M., Engelund, Morten Buch, Gripp, Karen W., Amlie‐Wolf, Louise, Henderson, Lindsay B., Midro, Alina T., Tarasów, Eugeniusz, Stasiewicz‐Jarocka, Beata, Moskal‐Jasinska, Diana, Vos, Paul, Boschann, Felix, Stoltenburg, Corinna, Puk, Oliver, Mero, Inger‐Lise, Lossius, Kristine, Mignot, Cyril, Keren, Boris, Acosta Guio, Johanna C., Briceño, Ignacio, Gomez, Alberto, Yang, Yaping, Stankiewicz, Pawel
Publicado en Am J Med Genet A (2021)

ALG1-CDG: Clinical and molecular characterization of 39 unreported patients

por Ng, Bobby G., Shiryaev, Sergey A., Rymen, Daisy, Eklund, Erik A., Raymond, Kimiyo, Kircher, Martin, Abdenur, Jose E., Alehan, Fusun, Midro, Alina T., Bamshad, Michael J., Barone, Rita, Berry, Gerard T., Brumbaugh, Jane E., Buckingham, Kati J., Clarkson, Katie, Cole, F. Sessions, O'Connor, Shawn, Cooper, Gregory M., Van Coster, Rudy, Demmer, Laurie A., Diogo, Luisa, Fay, Alexander J., Ficicioglu, Can, Fiumara, Agata, Gahl, William A., Ganetzky, Rebecca, Goel, Himanshu, Harshman, Lyndsay A., He, Miao, Jaeken, Jaak, James, Philip M., Katz, Daniel, Keldermans, Liesbeth, Kibaek, Maria, Kornberg, Andrew J., Lachlan, Katherine, Lam, Christina, Yaplito-Lee, Joy, Nickerson, Deborah A., Peters, Heidi L., Race, Valerie, Régal, Luc, Rush, Jeffrey S., Rutledge, S. Lane, Shendure, Jay, Souche, Erika, Sparks, Susan E., Trapane, Pamela, Sanchez-Valle, Amarilis, Vilain, Eric, Vøllo, Arve, Waechter, Charles J., Wang, Raymond Y., Wolfe, Lynne A., Wong, Derek A., Wood, Tim, Yang, Amy C., Matthijs, Gert, Freeze, Hudson H.
Publicado en Hum Mutat (2016)