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Showing results (11-20 of 31) with videos related to

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Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 1, 2003
Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesisAlexander Herr, Dominique Meunier, Ines Müller, et al.
Human Mutation|September 16, 2014
Integrated sequence analysis pipeline provides one-stop solution for identifying disease-causing mutationsHao Hu, Thomas F Wienker, Luciana Musante, et al.
Plos One|August 27, 2015
The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri FamiliesBehzad Davarniya, Hao Hu, Kimia Kahrizi, et al.
European Journal of Human Genetics : EJHG|December 21, 2006
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardationWei Chen, Lars R Jensen, Jozef Gecz, et al.
Human Molecular Genetics|July 9, 2005
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndromeUlrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.
Journal of Translational Medicine|September 24, 2004
BRCA1-mediated repression of select X chromosome genesAmir A Jazaeri, Gadisetti VR Chandramouli, Olga Aprelikova, et al.
European Journal of Human Genetics : EJHG|August 12, 2010
Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3Kimia Kahrizi, Cougar Hao Hu, Masoud Garshasbi, et al.
European Journal of Human Genetics : EJHG|February 27, 2014
A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disabilityFarzaneh Larti, Kimia Kahrizi, Luciana Musante, et al.
American Journal of Human Genetics|October 10, 2007
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsyHeather C Mefford, Severine Clauin, Andrew J Sharp, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 27, 2004
Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutationUmashankar Singh, Laurel E Fohn, Teruhiko Wakayama, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 1, 2003
Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesisAlexander Herr, Dominique Meunier, Ines Müller, et al.
Human Mutation|September 16, 2014
Integrated sequence analysis pipeline provides one-stop solution for identifying disease-causing mutationsHao Hu, Thomas F Wienker, Luciana Musante, et al.
Plos One|August 27, 2015
The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri FamiliesBehzad Davarniya, Hao Hu, Kimia Kahrizi, et al.
European Journal of Human Genetics : EJHG|December 21, 2006
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardationWei Chen, Lars R Jensen, Jozef Gecz, et al.
Human Molecular Genetics|July 9, 2005
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndromeUlrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.
Journal of Translational Medicine|September 24, 2004
BRCA1-mediated repression of select X chromosome genesAmir A Jazaeri, Gadisetti VR Chandramouli, Olga Aprelikova, et al.
European Journal of Human Genetics : EJHG|August 12, 2010
Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3Kimia Kahrizi, Cougar Hao Hu, Masoud Garshasbi, et al.
European Journal of Human Genetics : EJHG|February 27, 2014
A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disabilityFarzaneh Larti, Kimia Kahrizi, Luciana Musante, et al.
American Journal of Human Genetics|October 10, 2007
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsyHeather C Mefford, Severine Clauin, Andrew J Sharp, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 27, 2004
Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutationUmashankar Singh, Laurel E Fohn, Teruhiko Wakayama, et al.
Pageof 4