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Stem Cell Research|October 13, 2018
Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1Leonie Schipper, Deniz Kanber, Laura SteenpassBriefings in Functional Genomics|June 17, 2010
Imprinting of RB1 (the new kid on the block)Karin Buiting, Deniz Kanber, Bernhard Horsthemke, et al.Journal of Perinatal Medicine|August 9, 2019
Comparison of fetal cardiac functions between small-for-gestational age fetuses and late-onset growth-restricted fetusesBaşak Kaya, Ahmet Tayyar, Deniz Kanber Açar, et al.European Journal of Human Genetics : EJHG|October 23, 2008
Low frequency of imprinting defects in ICSI children born small for gestational ageDeniz Kanber, Karin Buiting, Michael Zeschnigk, et al.Stem Cell Research|April 9, 2020
Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC linesHannah Döpper, Marius Horstmann, Julia Menges, et al.Plos One|September 11, 2013
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1Laura Steenpass, Deniz Kanber, Michaela Hiber, et al.Echocardiography (Mount Kisco, N.Y.)|April 11, 2019
Prenatal diagnosis of left pulmonary artery sling and review of literatureSalim Sezer, Deniz Kanber Acar, Ali Ekiz, et al.Cancers|April 3, 2021
Introduction of a Variant Classification System for Analysis of Genotype-Phenotype Relationships in Heritable RetinoblastomaIsabel Hülsenbeck, Mirjam Frank, Eva Biewald, et al.Medical Ultrasonography|March 7, 2015
Prenatal diagnosis of congenital high airway obstruction syndrome (CHAOS). Five case reportHalil Aslan, Ali Ekiz, Deniz Kanber Acar, et al.European Journal of Human Genetics : EJHG|June 26, 2019
Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromesJasmin Beygo, Karin Buiting, Simon C Ramsden, et al.Pageof 5