Human Genetics logo Springer logo

Publisher: Springer

Related content
Volume 120, Number 4, November 2006

all issues

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

all issues

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page