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Optics Express|May 4, 2016
Nitride superluminescent diodes with broadened emission spectrum fabricated using laterally patterned substrateA Kafar, S Stanczyk, M Sarzynski, et al.
Journal of Applied Genetics|August 20, 2010
Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patientsK Czerska, A Sobczynska-Tomaszewska, D Sands, et al.
BMC Cancer|February 11, 2024
Identification and characterization of stromal-like cells with CD207+/low CD1a+/low phenotype derived from histiocytic lesions - a perspective in vitro model for drug testingAgnieszka Śmieszek, Klaudia Marcinkowska, Zofia Małas, et al.
Neonatology|January 24, 2015
High-Resolution Array Comparative Genomic Hybridization Utility in Polish Newborns with Isolated Cleft Lip and PalateKrzysztof Szczałuba, Beata A Nowakowska, Katarzyna Sobecka, et al.
Ginekologia Polska|January 15, 2021
Prenatal diagnosis of glutaric acidemia type 2 with the use of exome sequencing - an up-to-date review and new case reportAnna M Kucinska-Chahwan, Tomasz Roszkowski, Maciej Geremek, et al.
European Journal of Human Genetics : EJHG|August 19, 2010
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGHAnne Chun-Hui Tsai, Cherilyn J Dossett, Carol S Walton, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Severe mental retardation, seizures, and hypotonia due to deletions of MEF2CBeata A Nowakowska, Ewa Obersztyn, Krystyna Szymańska, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Journal of Medical Genetics|December 13, 2012
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSDonna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, et al.
European Journal of Human Genetics : EJHG|September 15, 2011
Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomaliesBeata A Nowakowska, Nicole de Leeuw, Claudia Al Ruivenkamp, et al.
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