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Deutsches Arzteblatt International|September 10, 2009
Polar body biopsy in the diagnosis of monogenic diseases: the birth of three healthy childrenGeorg Griesinger, Nana Bündgen, Diana Salmen, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxiasAndreas Dalski, Jassemien Atici, Friedmar R Kreuz, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 11, 2003
Chromatin preferences of the perichromosomal layer constituent pKi-67Walther Traut, Elmar Endl, Silvia Garagna, et al.
American Journal of Respiratory and Critical Care Medicine|March 8, 2005
Study of C-C chemokine receptor 2 alleles in sarcoidosis, with emphasis on family-based analysisRuta Valentonyte, Jochen Hampe, Peter J P Croucher, et al.
Journal of Neurology|May 28, 2004
Aprataxin mutations are a rare cause of early onset ataxia in GermanyMatthias Habeck, Christine Zühlke, Karl H P Bentele, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
Polar body diagnosis for hemophilia a using multiplex PCR for linked polymorphic markersDiana Tomi, Georg Griesinger, Askan Schultze-Mosgau, et al.
Human Mutation|April 23, 2002
Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genesKerstin Kutsche, Bernadette Ressler, Heide-Gertrude Katzera, et al.
Human Mutation|February 22, 2002
Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1DBenigna von Brederlow, Hanno Bolz, Andreas Janecke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 7, 2006
Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?Ana Djarmati, Katja Hedrich, Marina Svetel, et al.
American Journal of Human Genetics|December 1, 2001
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectivelyDebra A Thompson, Christina L McHenry, Yun Li, et al.
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