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A Rappold

Showing results (101-110 of 160) with videos related to

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Plos One|May 27, 2015
Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortexXue Li, Jian Xiao, Henning Fröhlich, et al.
Journal of Medical Genetics|November 15, 2015
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani familyRafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Human Genetics|August 1, 1997
FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomesE Rao, B Weiss, M Fukami, et al.
Genes|September 4, 2020
Two Cases of Recessive Intellectual Disability Caused by <i>NDST1</i> and <i>METTL23</i> VariantsAmjad Khan, Zhichao Miao, Muhammad Umair, et al.
Hormone Research in Paediatrics|March 4, 2010
Hormones and genes of importance in bone physiology and their influence on bone mineralization and growth in Turner syndromeAnenisia C Andrade, Jeffrey Baron, Stavros C Manolagas, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short statureGudrun A Rappold, Maki Fukami, Beate Niesler, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Phenotypic variation and genetic heterogeneity in Léri-Weill syndromeS Schiller, S Spranger, B Schechinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2002
The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardationVolker Endris, Birgit Wogatzky, Uwe Leimer, et al.
The Annals of Otology, Rhinology, and Laryngology|February 25, 2003
Congenital conductive hearing loss in dyschondrosteosisEls M R De Leenheer, Grétel G Oudesluijs, Anne-Marie Kuijpers-Jagtman, et al.
Pageof 16

Showing results (101-110 of 160) with videos related to

Sort By:
Pageof 16
Plos One|May 27, 2015
Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortexXue Li, Jian Xiao, Henning Fröhlich, et al.
Journal of Medical Genetics|November 15, 2015
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani familyRafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Human Genetics|August 1, 1997
FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomesE Rao, B Weiss, M Fukami, et al.
Genes|September 4, 2020
Two Cases of Recessive Intellectual Disability Caused by <i>NDST1</i> and <i>METTL23</i> VariantsAmjad Khan, Zhichao Miao, Muhammad Umair, et al.
Hormone Research in Paediatrics|March 4, 2010
Hormones and genes of importance in bone physiology and their influence on bone mineralization and growth in Turner syndromeAnenisia C Andrade, Jeffrey Baron, Stavros C Manolagas, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short statureGudrun A Rappold, Maki Fukami, Beate Niesler, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Phenotypic variation and genetic heterogeneity in Léri-Weill syndromeS Schiller, S Spranger, B Schechinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2002
The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardationVolker Endris, Birgit Wogatzky, Uwe Leimer, et al.
The Annals of Otology, Rhinology, and Laryngology|February 25, 2003
Congenital conductive hearing loss in dyschondrosteosisEls M R De Leenheer, Grétel G Oudesluijs, Anne-Marie Kuijpers-Jagtman, et al.
Pageof 16