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H G Brunner

Showing results (151-160 of 179) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Genotype versus phenotype in families with androgen insensitivity syndromeA L Boehmer, O Brinkmann, H Brüggenwirth, et al.
Genes, Brain, and Behavior|August 19, 2014
A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrusD-C Cai, H Fonteijn, T Guadalupe, et al.
Journal of Medical Genetics|April 5, 2005
Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndromeT Kleefstra, M Smidt, M J G Banning, et al.
Cell|October 27, 1999
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.
Molecular Psychiatry|July 25, 2007
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsyJ I Friedman, T Vrijenhoek, S Markx, et al.
Human Molecular Genetics|February 13, 2001
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63J A McGrath, P H Duijf, V Doetsch, et al.
Human Molecular Genetics|September 1, 1996
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.
American Journal of Human Genetics|July 1, 1996
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13Y Gong, M Vikkula, L Boon, et al.
American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Pageof 18

Showing results (151-160 of 179) with videos related to

Sort By:
Pageof 18
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Genotype versus phenotype in families with androgen insensitivity syndromeA L Boehmer, O Brinkmann, H Brüggenwirth, et al.
Genes, Brain, and Behavior|August 19, 2014
A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrusD-C Cai, H Fonteijn, T Guadalupe, et al.
Journal of Medical Genetics|April 5, 2005
Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndromeT Kleefstra, M Smidt, M J G Banning, et al.
Cell|October 27, 1999
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.
Molecular Psychiatry|July 25, 2007
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsyJ I Friedman, T Vrijenhoek, S Markx, et al.
Human Molecular Genetics|February 13, 2001
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63J A McGrath, P H Duijf, V Doetsch, et al.
Human Molecular Genetics|September 1, 1996
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.
American Journal of Human Genetics|July 1, 1996
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13Y Gong, M Vikkula, L Boon, et al.
American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Pageof 18