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American Journal of Human Genetics|October 9, 2002
The DNA-based structure of human chromosome 5 in interphaseJohannes Lemke, Jan Claussen, Susanne Michel, et al.European Journal of Human Genetics : EJHG|October 4, 2012
Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defectsMaria Arélin, Bernt Schulze, Bertram Müller-Myhsok, et al.Nucleus (Austin, Tex.)|February 18, 2011
Dosage effect of zero to three functional LBR-genes in vivo and in vitroSophia Gravemann, Nele Schnipper, Hannes Meyer, et al.Human Mutation|December 24, 2002
Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10Barbara Zoll, Lars Petersen, Katrin Lange, et al.Journal of Medical Genetics|December 2, 2009
Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in humanSascha Tierling, Nicole Y Souren, Jasmin Gries, et al.Human Molecular Genetics|December 20, 2002
Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomalyLeonard D Shultz, Bonnie L Lyons, Lisa M Burzenski, et al.Scientific Reports|October 4, 2018
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiationManuel Holtgrewe, Alexej Knaus, Gabriele Hildebrand, et al.Human Genetics|May 10, 2022
Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4Heidemarie Neitzel, Raymonda Varon, Sana Chughtai, et al.Cell Cycle (Georgetown, Tex.)|August 23, 2011
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephalyJuan Alberto Marchal, Mahdi Ghani, Detlev Schindler, et al.International Journal of Cancer|June 9, 2004
Increased cancer risk of heterozygotes with NBS1 germline mutations in PolandJan Steffen, Raymonda Varon, Maria Mosor, et al.Pageof 7