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3 documents found
1: Title: Molecular and clinical delineation of the 17q22 microdeletion phenotype.
Authors: Laurell, Tobias, et.al. .
Journal: European journal of human genetics : EJHG (Eur J Hum Genet), Vol. 21 (10): 1085-92, 2013 .
Snippet: We show that the commonly deleted region in our patients spans 0.24 Mb and two genes; NOG and C17ORF67.
Affiliation: 1] Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden [2] Department of Molecular Medicine and Surgery and Center of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden [3] Department of Hand Surgery, Södersjukhuset, Stockholm, Sweden. .
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2: Title: Association between genetic determinants of peak height velocity during puberty and predisposition to adolescent idiopathic scoliosis.
Authors: Mao, Saihu, et.al. .
Journal: Spine, Vol. 38 (12): 1034-9, 2013 .
Snippet: RESULTS: Strong associations between rs12459350 in DOT1L, rs4794665 in C17orf67, and susceptibility of AIS were found, with the PHV increasing allele G of rs12459350 and PHV/adult height increasing allele A of rs4794665 both being significant predisposition alleles of AIS (P = 0.001 for rs12459350, odds ratio = 1.16, 95% confidence interval = 1.06-1.27;
Affiliation: *Department of Spine Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China; and †Jiangsu Key Laboratory for Molecular Medicine, Nanjing University Medical School, Nanjing, China. .
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3: Title: Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966.
Authors: Sovio, Ulla, et.al. .
Journal: PLoS genetics (Plos Genet), Vol. 5 (3): e1000409, 2009 .
Snippet: Seven SNPs in or near the genes HHIP, DLEU7, UQCC, SF3B4/SV2A, LCORL, and HIST1H1D associated with PHV1 and five SNPs in or near SOCS2, SF3B4/SV2A, C17orf67, CABLES1, and DOT1L with PHV2 (p<0.05).
Affiliation: Department of Epidemiology and Public Health, Imperial College London, London, United Kingdom. .
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