Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Epilepsy & Behavior Reports|January 11, 2021
STX1B-related epilepsy in a 24-month-old female infantKatharina Burghardt, Naomi Baba, Isolde Schreyer, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotypeIsolde Schreyer, Annett Neumann, Volkmar Beensen, et al.
Journal of Prenatal Medicine|July 1, 2016
Alpha-fetoprotein and its value for predicting pregnancy outcomes - a re-evaluationAyham Alhaj Darouich, Thomas Liehr, Anja Weise, et al.
Molecular Cytogenetics|May 13, 2022
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypesNaomi Baba, Anna Lengyel, Eva Pinti, et al.
Molecular Medicine Reports|April 8, 2011
Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case reportHeike Nelle, Isolde Schreyer, Elisabeth Ewers, et al.
Molecular Cytogenetics|March 16, 2018
Parental origin of deletions and duplications - about the necessity to check for cryptic inversionsThomas Liehr, Isolde Schreyer, Alma Kuechler, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2007
New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bankHolger Tönnies, Joanna Pietrzak, Ewa Bocian, et al.
Human Genetics|September 19, 2003
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classificationHeike Starke, Angela Nietzel, Anja Weise, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopiaMax Lange, Burkhard Kasper, Axel Bohring, et al.
International Journal of Molecular Medicine|May 29, 2008
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literatureMarina Manvelyan, Mariluce Riegel, Monica Santos, et al.
Pageof 2