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Peter Nürnberg

Showing results (171-180 of 517) with videos related to

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American Journal of Medical Genetics. Part A|March 23, 2017
Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2Shahida Moosa, Annette Haagerup, Pernille Axel Gregersen, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 21, 2004
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutationsMarkus Pfister, Holger Thiele, Guy Van Camp, et al.
Human Genetics|May 20, 2020
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndromeRoser Ufartes, Hanna Berger, Katharina Till, 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.
Genome Research|December 25, 2019
Identification of pathogenic variant enriched regions across genes and gene familiesEduardo Pérez-Palma, Patrick May, Sumaiya Iqbal, et al.
Nature Genetics|January 31, 2002
A comprehensive linkage analysis for myocardial infarction and its related risk factorsUlrich Broeckel, Christian Hengstenberg, Björn Mayer, et al.
Pediatrics|February 4, 2003
Genome scan for childhood and adolescent obesity in German familiesKathrin Saar, Frank Geller, Franz Rüschendorf, et al.
American Journal of Human Genetics|March 29, 2002
Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36Maria J Schuermann, Edgar Otto, Achim Becker, et al.
Journal of Clinical Microbiology|May 5, 2006
Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantationJuergen Loeffler, Michael Steffens, Eva-Maria Arlt, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|September 18, 2013
Fine mapping and chromosome walking towards the Ror1 locus in barley (Hordeum vulgare L.)Johanna Acevedo-Garcia, Nicholas C Collins, Nahal Ahmadinejad, et al.
Pageof 52

Showing results (171-180 of 517) with videos related to

Sort By:
Pageof 52
American Journal of Medical Genetics. Part A|March 23, 2017
Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2Shahida Moosa, Annette Haagerup, Pernille Axel Gregersen, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 21, 2004
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutationsMarkus Pfister, Holger Thiele, Guy Van Camp, et al.
Human Genetics|May 20, 2020
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndromeRoser Ufartes, Hanna Berger, Katharina Till, 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.
Genome Research|December 25, 2019
Identification of pathogenic variant enriched regions across genes and gene familiesEduardo Pérez-Palma, Patrick May, Sumaiya Iqbal, et al.
Nature Genetics|January 31, 2002
A comprehensive linkage analysis for myocardial infarction and its related risk factorsUlrich Broeckel, Christian Hengstenberg, Björn Mayer, et al.
Pediatrics|February 4, 2003
Genome scan for childhood and adolescent obesity in German familiesKathrin Saar, Frank Geller, Franz Rüschendorf, et al.
American Journal of Human Genetics|March 29, 2002
Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36Maria J Schuermann, Edgar Otto, Achim Becker, et al.
Journal of Clinical Microbiology|May 5, 2006
Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantationJuergen Loeffler, Michael Steffens, Eva-Maria Arlt, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|September 18, 2013
Fine mapping and chromosome walking towards the Ror1 locus in barley (Hordeum vulgare L.)Johanna Acevedo-Garcia, Nicholas C Collins, Nahal Ahmadinejad, et al.
Pageof 52