Cytogenomic characteristics of murine breast cancer cell line JC

por Azawi, Shaymaa, Rincic, Martina, Liehr, Thomas
Publicado 2021

Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting

por Rinčić, Martina, Iourov, Ivan Y., Liehr, Thomas
Publicado 2016

Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka

por Azawi, Shaymaa, Liehr, Thomas, Rincic, Martina, Manferrari, Mattia
Publicado 2020

Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

por Wahlbuhl, Eva, Liehr, Thomas, Rincic, Martina, Azawi, Shaymaa
Publicado 2020

7p21.3 Together With a 12p13.32 Deletion in a Patient With Microcephaly—Does 12p13.32 Locus Possibly Comprises a Candidate Gene Region for Microcephaly?

por Rincic, Martina, Rados, Milan, Kopic, Janja, Krsnik, Zeljka, Liehr, Thomas
Publicado 2021

Molecular cytogenetic characterization of the urethane-induced murine lung cell line LA-4 as a model for human squamous cell lung cancer

por Azawi, Shaymaa, Balachandran, Milash, Kramer, Fritz, Kankel, Stefanie, Rincic, Martina, Liehr, Thomas
Publicado 2022

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex

por Rincic, Martina, Rados, Milan, Krsnik, Zeljka, Gotovac, Kristina, Borovecki, Fran, Liehr, Thomas, Brecevic, Lukrecija
Publicado 2016

Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH)

por Alhourani, Eyad, Rincic, Martina, Othman, Moneeb AK, Pohle, Beate, Schlie, Cordula, Glaser, Anita, Liehr, Thomas
Publicado 2014

Isochromosome 17q in Chronic Lymphocytic Leukemia

por Alhourani, Eyad, Rincic, Martina, Melo, Joana B., Carreira, Isabel M., Glaser, Anita, Pohle, Beate, Schlie, Cordula, Liehr, Thomas
Publicado 2015

Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach...

por Brečević, Lukrecija, Rinčić, Martina, Krsnik, Željka, Sedmak, Goran, Hamid, Ahmed B., Kosyakova, Nadezda, Galić, Ivan, Liehr, Thomas, Borovečki, Fran
Publicado 2015

A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia

por Othman, Moneeb A. K., Rincic, Martina, Melo, Joana B., Carreira, Isabel M., Alhourani, Eyad, Hunstig, Friederike, Glaser, Anita, Liehr, Thomas
Publicado 2014

European registration process for Clinical Laboratory Geneticists in genetic healthcare

por Liehr, Thomas, Carreira, Isabel M, Aktas, Dilek, Bakker, Egbert, Rodríguez de Alba, Marta, Coviello, Domenico A, Florentin, Lina, Scheffer, Hans, Rincic, Martina
Publicado 2017

Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries

por Liehr, Thomas, Carreira, Isabel M., Balogh, Zsofia, Garrido, Elena Dominguez, Verdorfer, Irmgard, Coviello, Domenico A., Florentin, Lina, Scheffer, Hans, Rincic, Martina, Williams, Heather E.
Publicado 2019

High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia

por Othman, Moneeb A. K., Melo, Joana B., Carreira, Isabel M., Rincic, Martina, Glaser, Anita, Grygalewicz, Beata, Gruhn, Bernd, Wilhelm, Kathleen, Rittscher, Katharina, Meyer, Britta, Silva, Maria Luiza Macedo, de Jesus Marques Salles, Terezinha, Liehr, Thomas
Publicado 2015