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Klinische Padiatrie|July 1, 1985
Ring chromosome 4 : 46,XY, r(4) (p16q35) in a boyA Gutkowska, M Krajewska-Walasek, L WiśniewskiActa Geneticae Medicae Et Gemellologiae|January 1, 1996
A new case of Beckwith-Wiedemann syndrome with an 11p15 duplication of paternal origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat]M Krajewska-Walasek, A Gutkowska, M Mospinek-Krasnopolska, et al.Klinische Padiatrie|March 1, 1984
9p-syndrome: two new observationsJ Szymańska, A Gutkowska, J Kubalska, et al.Clinical Genetics|September 4, 1998
A case of Prader-Willi syndrome arising as a result of familial unbalanced translocation t(11;15)(q25;q13)M Krajewska Walasek, A Gutkowska, B Bielińska, et al.European Journal of Pediatrics|March 1, 1985
A new case of partial trisomy of 17 long arm. Densitometric analysis of aberrationsB Parcheta, W Skawiński, L Wiśniewski, et al.Pediatria Polska|October 1, 1995
[Diagnosis of Edwards syndrome in newborns]D Dunin-Wasowicz, M Krajewska-Walasek, K Rowecka-Trzebicka, et al.American Journal of Medical Genetics|September 25, 2001
Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 geneP Stankiewicz, J Rujner, C Löffler, et al.American Journal of Medical Genetics|July 3, 1995
Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndromeK H Chrzanowska, W J Kleijer, M Krajewska-Walasek, et al.Journal of Medical Genetics|April 4, 2000
Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplicationsD Kotzot, M J Martinez, G Bagci, et al.Pageof 1