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Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|July 2, 2003
Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISHAlma Kuechler, Mareike Dreidax, Steffi U Pigorsch, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injectionAlma Kuechler, Monika Ziegler, Cornelia Blank, et al.
American Journal of Medical Genetics. Part A|January 12, 2013
Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations in ABCC9Johanna Christina Czeschik, Claudia Voigt, Timm O Goecke, et al.
Frontiers in Pediatrics|March 6, 2024
Distinct neonatal hyperammonemia and liver synthesis dysfunction: case report of a severe MEGDHEL syndromeIna Kirchberg, Elke Lainka, Andrea Gangfuß, et al.
International Journal of Molecular Medicine|March 14, 2002
Microdissection based high resolution multicolor banding for all 24 human chromosomesThomas Liehr, Anita Heller, Heike Starke, et al.
European Journal of Human Genetics : EJHG|December 11, 2008
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeDeniz Kanber, Jacques Giltay, Dagmar Wieczorek, et al.
Molecular Cytogenetics|August 8, 2020
13q deletion syndrome resulting from balanced chromosomal rearrangement in father: the significance of parental karyotypingSabine Dittner-Moormann, Madlen Reschke, Eva Biewald, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|December 29, 2006
Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genesMichael Glei, Anja Schaeferhenrich, Uwe Claussen, et al.
European Journal of Human Genetics : EJHG|February 6, 2021
Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathyJohann Kaspar Lieberwirth, Pascal Joset, Anja Heinze, et al.
American Journal of Medical Genetics. Part A|May 16, 2015
ADAMTSL4-associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype descriptionTeresa M Neuhann, Annette Stegerer, Angelika Riess, et al.
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