TABLE OF CONTENTS
Volume 50, Issue 3 (March 2005)
Original Articles
DNase II polymorphisms associated with risk of renal disorder among systemic lupus erythematosus patients
Hyoung Doo Shin, Byung Lae Park, Hyun Sup Cheong, Hye-Soon Lee, Jae-Bum Jun and Sang-Cheol Bae
J Hum Genet 50: 107-111; advance online publication, February 19, 2005; doi:10.1007/s10038-004-0227-3
Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion
Sami Tsukishiro, Qing Ying Li, Mitsuyo Tanemura, Mayumi Sugiura-Ogasawara, Kaoru Suzumori and Shin-ichi Sonta
J Hum Genet 50: 112-117; advance online publication, March 4, 2005; doi:10.1007/s10038-005-0229-9
Association of eotaxin-2 gene polymorphisms with plasma eotaxin-2 concentration
Ji-Won Min, June-Hyuk Lee, Choon-Sik Park, Hun Soo Chang, Tai Youn Rhim, Sung-Woo Park, An-Soo Jang and Hyoung-Doo Shin
J Hum Genet 50: 118-123; advance online publication, March 3, 2005; doi:10.1007/s10038-005-0230-3
Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells
Masayuki Haruta, Makiko Meguro, Yu-ki Sakamoto, Hidetoshi Hoshiya, Akiko Kashiwagi, Yasuhiko Kaneko, Kohzoh Mitsuya and Mitsuo Oshimura
J Hum Genet 50: 124-132; advance online publication, March 3, 2005; doi:10.1007/s10038-005-0231-2
Association analysis of signal transducer and activator of transcription 4 (STAT4) polymorphisms with asthma
Byung Lae Park, Hyun Sub Cheong, Lyoung Hyo Kim, Yoo Hyun Choi, Sohg Namgoong, Hae-Sim Park, Soo-Jong Hong, Byoung Whui Choi, June Hyuk Lee, Choon-Sik Park and Hyoung Doo Shin
J Hum Genet 50: 133-138; advance online publication, March 3, 2005; doi:10.1007/s10038-005-0232-1
Parallel minisequencing followed by multiplex matrix-assisted laser desorption/ionization mass spectrometry assay for 
-thalassemia mutations
Hsin-Kai Liao, Yi-Ning Su, Hung-Yi Kao, Chia-Cheng Hung, Hsueh-Ting Wang and Yu-Ju Chen
J Hum Genet 50: 139-150; advance online publication, March 11, 2005; doi:10.1007/s10038-005-0234-z
Short Communications
Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects
Andrew J Ridley, James Colley, David Wynford-Thomas and Christopher J Jones
J Hum Genet 50: 151-154; advance online publication, March 3, 2005; doi:10.1007/s10038-004-0228-2
Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family
Uma Mittal, Sanghamitra Roy, Satish Jain, Achal K Srivastava and Mitali Mukerji
J Hum Genet 50: 155-157; advance online publication, March 5, 2005; doi:10.1007/s10038-005-0233-0
