Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|February 25, 2017
Targeted prenatal diagnosis of Pallister-Killian syndromeAnna Kucińska-Chahwan, Julia Bijok, Sylwia Dąbkowska, et al.
Archives of Gynecology and Obstetrics|May 13, 2022
Prenatal diagnosis of acrania/exencephaly/anencephaly sequence (AEAS): additional structural and genetic anomaliesJulia Bijok, Sylwia Dąbkowska, Anna Kucińska-Chahwan, et al.
Medycyna Wieku Rozwojowego|October 10, 2006
[Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations]Ewa Bocian, Beata Nowakowska, Ewa Obersztyn, et al.
Polski Merkuriusz Lekarski : Organ Polskiego Towarzystwa Lekarskiego|May 4, 2016
[17p13.3 duplication as a cause of psychomotor developmental delay in an infant - a further case of a new syndrome]Amanda Przybylska-Kruszewska, Anna Kutkowska-Kaźmierczak, Amanda Krzywdzińska, et al.
American Journal of Medical Genetics. Part A|July 17, 2007
A girl with deletion 9q22.1-q22.32 including the PTCH and ROR2 genes identified by genome-wide array-CGHBeata Nowakowska, Anna Kutkowska-Kaźmierczak, Paweł Stankiewicz, et al.
American Journal of Medical Genetics. Part A|October 17, 2007
Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardationKatarzyna Borg, Beata Nowakowska, Ewa Obersztyn, et al.
Medycyna Wieku Rozwojowego|October 20, 2009
[Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods]Katarzyna Borg, Ewa Bocian, Joanna Bernaciak, et al.
American Journal of Clinical Pathology|December 23, 2017
The 11q-Gain/Loss Aberration Occurs Recurrently in MYC-Negative Burkitt-like Lymphoma With 11q Aberration, as Well as MYC-Positive Burkitt Lymphoma and MYC-Positive High-Grade B-Cell Lymphoma, NOSBeata Grygalewicz, Renata Woroniecka, Grzegorz Rymkiewicz, et al.
Cancer Genetics|June 13, 2020
Genetic progression of post-transplant Burkitt-like lymphoma case with 11q-Gain/Loss and MYC amplificationBeata Grygalewicz, Renata Woroniecka, Grzegorz Rymkiewicz, et al.
American Journal of Medical Genetics. Part A|March 11, 2015
Co-segregation of Freiberg's infraction with a familial translocation t(5;7)(p13.3;p22.2) ascertained by a child with cri du chat syndrome and brachydactyly type A1BMarta Myśliwiec, Barbara Panasiuk, Maria Dębiec-Rychter, et al.
Pageof 6