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Han G Brunner

Showing results (31-40 of 318) with videos related to

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Biological Psychiatry|July 20, 2010
Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individualsBarbara Franke, Alejandro Arias Vasquez, Joris A Veltman, et al.
European Journal of Human Genetics : EJHG|February 24, 2006
A text-mining analysis of the human phenomeMarc A van Driel, Jorn Bruggeman, Gert Vriend, et al.
Journal of Genetic Counseling|November 11, 2022
Clinical geneticists' views on and experiences with unsolicited findings in next-generation sequencing: "A great technology creating new dilemmas"Vyne van der Schoot, Carlijn Damsté, Helger G Yntema, et al.
Neurobiology of Aging|July 6, 2011
CR1 genotype is associated with entorhinal cortex volume in young healthy adultsJanita Bralten, Barbara Franke, Alejandro Arias-Vásquez, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA)Cecilia Giunta, Ann Randolph, Lihadh I Al-Gazali, et al.
Brain Research. Developmental Brain Research|July 6, 2005
Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresisBert van der Zwaag, J Peter H Burbach, Han G Brunner, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
Clinical Dysmorphology|September 5, 2009
Choanal atresia, syngnathia, brachydactyly, mental retardation and short stature: an X-linked syndrome?Marjolijn C J Jongmans, Rolph Pfundt, Jayne Y Hehir-Kwa, et al.
Iranian Biomedical Journal|May 4, 2017
Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration FamiliesMohammad Ghofrani, Mahin Yahyaei, Han G. Brunner, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A new web-based data mining tool for the identification of candidate genes for human genetic disordersMarc A van Driel, Koen Cuelenaere, Patrick P C W Kemmeren, et al.
Pageof 32

Showing results (31-40 of 318) with videos related to

Sort By:
Pageof 32
Biological Psychiatry|July 20, 2010
Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individualsBarbara Franke, Alejandro Arias Vasquez, Joris A Veltman, et al.
European Journal of Human Genetics : EJHG|February 24, 2006
A text-mining analysis of the human phenomeMarc A van Driel, Jorn Bruggeman, Gert Vriend, et al.
Journal of Genetic Counseling|November 11, 2022
Clinical geneticists' views on and experiences with unsolicited findings in next-generation sequencing: "A great technology creating new dilemmas"Vyne van der Schoot, Carlijn Damsté, Helger G Yntema, et al.
Neurobiology of Aging|July 6, 2011
CR1 genotype is associated with entorhinal cortex volume in young healthy adultsJanita Bralten, Barbara Franke, Alejandro Arias-Vásquez, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA)Cecilia Giunta, Ann Randolph, Lihadh I Al-Gazali, et al.
Brain Research. Developmental Brain Research|July 6, 2005
Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresisBert van der Zwaag, J Peter H Burbach, Han G Brunner, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
Clinical Dysmorphology|September 5, 2009
Choanal atresia, syngnathia, brachydactyly, mental retardation and short stature: an X-linked syndrome?Marjolijn C J Jongmans, Rolph Pfundt, Jayne Y Hehir-Kwa, et al.
Iranian Biomedical Journal|May 4, 2017
Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration FamiliesMohammad Ghofrani, Mahin Yahyaei, Han G. Brunner, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A new web-based data mining tool for the identification of candidate genes for human genetic disordersMarc A van Driel, Koen Cuelenaere, Patrick P C W Kemmeren, et al.
Pageof 32