Search Results - Bonin, Michael

Expression of genes related to germ cell lineage and pluripotency in single cells and colonies of human adult germ stem cells by Conrad, Sabine (Author) , Azizi, Hossein (Author) , Hatami, Maryam (Author) , Kubista, Mikael (Author) , Bonin, Michael (Author) , Hennenlotter, Jörg (Author) , Sievert, Karl-Dietrich (Author) , Skutella, Thomas (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Genome-wide UPD screening in patients with intellectual disability by Schroeder, Christopher Maximilian (Author) , Ekici, Arif Bülent (Author) , Moog, Ute (Author) , Grasshoff, Ute (Author) , Mau-Holzmann, Ulrike (Author) , Sturm, Marc (Author) , Vosseler, Vanessa (Author) , Poths, Sven (Author) , Rappold, Gudrun (Author) , Riess, Angelika (Author) , Riess, Olaf (Author) , Dufke, Andreas (Author) , Bonin, Michael (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability by Gazou, Anastasia (Author) , Riess, Angelika (Author) , Grasshoff, Ute (Author) , Schäferhoff, Karin (Author) , Bonin, Michael (Author) , Jauch, Anna (Author) , Riess, Olaf (Author) , Tzschach, Andreas (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes

De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation by Grasshoff, Ute (Author) , Bonin, Michael (Author) , Goehring, Ina (Author) , Ekici, Arif (Author) , Dufke, Andreas (Author) , Cremer, Kirsten (Author) , Wagner, Nicholas (Author) , Rossier, Eva (Author) , Jauch, Anna (Author) , Walter, Michael (Author) , Bauer, Claudia (Author) , Bauer, Peter (Author) , Horber, Karl (Author) , Beck-Woedl, Stefanie (Author) , Wieczorek, Dagmar (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation by Berkel, Simone (Author) , Marshall, Christian R. (Author) , Weiß, Birgit (Author) , Howe, Jennifer (Author) , Röth, Ralph (Author) , Moog, Ute (Author) , Endris, Volker (Author) , Roberts, Wendy (Author) , Szatmari, Peter (Author) , Pinto, Dalila (Author) , Bonin, Michael (Author) , Riess, Angelika (Author) , Engels, Hartmut (Author) , Sprengel, Rolf (Author) , Scherer, Stephen W. (Author) , Rappold, Gudrun (Author) ,

Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia by Endris, Volker (Author) , Hackmann, Karl (Author) , Neuhann, Teresa M. (Author) , Grasshoff, Ute (Author) , Bonin, Michael (Author) , Haug, Ulrich (Author) , Hahn, Gabriele (Author) , Schallner, Jens C. (Author) , Schröck, Evelin (Author) , Tinschert, Sigrid (Author) , Rappold, Gudrun (Author) , Moog, Ute (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits by Horn, Denise (Author) , Kapeller, Johannes (Author) , Rivera-Brugués, Núria (Author) , Moog, Ute (Author) , Lorenz-Depiereux, Bettina (Author) , Eck, Sebastian (Author) , Hempel, Maja (Author) , Wagenstaller, Janine (Author) , Gawthrope, Alex (Author) , Monaco, Anthony P. (Author) , Bonin, Michael (Author) , Riess, Olaf (Author) , Wohlleber, Eva (Author) , Illig, Thomas (Author) , Bezzina, Connie R. (Author) , Franke, Andre (Author) , Spranger, Stephanie (Author) , Villavicencio-Lorini, Pablo (Author) , Seifert, Wenke (Author) , Rosenfeld, Jochen (Author) , Klopocki, Eva (Author) , Rappold, Gudrun (Author) , Strom, Tim M. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext