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Medycyna Wieku Rozwojowego|October 30, 2007
[Clinical manifestation of chromosome 2 long arm terminal deletion--presentation of four cases]Krzysztof Szczałuba, Ewa Obersztyn, Kamila Ziemkiewicz, et al.Clinical Dysmorphology|December 8, 2020
Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?Aleksandra Jezela-Stanek, Paulina Pokora, Marlena Młynek, et al.Molecular Syndromology|March 22, 2016
Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II ErrorsRon Hochstenbach, Beata Nowakowska, Marianne Volleth, et al.Journal of Applied Genetics|December 4, 2013
Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disabilityMagdalena Bartnik, Beata Nowakowska, Katarzyna Derwińska, et al.Genes|March 29, 2023
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion SyndromeMarta Smyk, Maciej Geremek, Kamila Ziemkiewicz, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 25, 2012
Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disordersMagdalena Bartnik, Elżbieta Szczepanik, Katarzyna Derwińska, et al.Genes|April 23, 2022
Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 PregnanciesKatarzyna Kowalczyk, Magdalena Bartnik-Głaska, Marta Smyk, et al.Pageof 1