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Volume 120, Number 4, November 2006

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The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males
pp. 447-459(13)
Authors: Rosenberg, Shai; Templeton, Alan; Feigin, Paul; Lancet, Doron; Beckmann, Jacques; Selig, Sara; Hamer, Dean; Skorecki, Karl

Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts
pp. 487-499(13)
Authors: Machuca-Tzili, Laura; Thorpe, Helena; Robinson, Thelma; Sewry, Caroline; Brook, J.

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations
pp. 501-518(18)
Authors: Beaty, T.; Hetmanski, J.; Fallin, M.; Park, J.; Sull, J.; McIntosh, I.; Liang, K.; VanderKolk, C.; Redett, R.; Boyadjiev, S.; Jabs, E.; Chong, S.; Cheah, F.; Wu-Chou, Y.; Chen, P.; Chiu, Y.; Yeow, V.; Ng, I.; Cheng, J.; Huang, S.; Ye, X.; Wang, H.; Ingersoll, R.; Scott, A.

Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations
pp. 519-526(8)
Authors: Gajecka, Marzena; Pavlicek, Adam; Glotzbach, Caron; Ballif, Blake; Jarmuz, Malgorzata; Jurka, Jerzy; Shaffer, Lisa

Association study on chromosome 20q11.21-13.13 locus and its contribution to type 2 diabetes susceptibility in Japanese
pp. 527-542(16)
Authors: Tanahashi, Toshihito; Osabe, Dai; Nomura, Kyoko; Shinohara, Shuichi; Kato, Hitoshi; Ichiishi, Eiichiro; Nakamura, Naoto; Yoshikawa, Toshikazu; Takata, Yoichiro; Miyamoto, Tatsuro; Shiota, Hiroshi; Keshavarz, Parvaneh; Yamaguchi, Yuka; Kunika, Kiyoshi; Moritani, Maki; Inoue, Hiroshi; Itakura, Mitsuo

A shared Y-chromosomal heritage between Muslims and Hindus in India
pp. 543-551(9)
Authors: Gutala, Ramana; Carvalho-Silva, Denise; Jin, Li; Yngvadottir, Bryndis; Avadhanula, Vasanthi; Nanne, Khaja; Singh, Lalji; Chakraborty, Ranajit; Tyler-Smith, Chris

Potential effect on cellular response to cadmium of a single-nucleotide A → G polymorphism in the promoter of the human gene for metallothionein IIA
pp. 553-560(8)
Authors: Kita, Kayoko; Miura, Nobuhiko; Yoshida, Minoru; Yamazaki, Kentaro; Ohkubo, Takayoshi; Imai, Yutaka; Naganuma, Akira

Bias, precision and heritability of self-reported and clinically measured height in Australian twins
pp. 571-580(10)
Authors: Macgregor, Stuart; Cornes, Belinda; Martin, Nicholas; Visscher, Peter

The fatty acid amide hydrolase 385 A/A (P129T) variant: haplotype analysis of an ancient missense mutation and validation of risk for drug addiction
pp. 581-588(8)
Authors: Flanagan, Jonathan; Gerber, Alexandra; Cadet, Jean; Beutler, Ernest; Sipe, Jack

Novel aminoglycosides increase SMN levels in spinal muscular atrophy fibroblasts
pp. 589-601(13)
Authors: Mattis, Virginia; Rai, Ravi; Wang, Jinhua; Chang, Cheng-Wei; Coady, Tristan; Lorson, Christian

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