Annals of Human Genetics

Fatal Malonyl CoA Decarboxylase Deficiency Due to Maternal Uniparental Isodisomy of the Telomeric End of Chromosome 16
pp. 705-712(8)
Authors: Malvagia, S.; Papi, L.; Morrone, A.; Donati, M. A.; Ciani, F.; Pasquini, E.; la Marca, G.; Scholte, H. R.; Genuardi, M.; Zammarchi, E.

Leukocyte cDNA Analysis of NSD1 Derived from Confirmed Sotos Syndrome Patients
pp. 713-718(6)
Authors: Duno, M.; Skovby, F.; Schwartz, M.

The Impact of BRCA1 on Spina Bifida Meningomyelocele Lesions
pp. 719-728(10)
Authors: King, Terri M.; Au, Kit-Sing; Kirkpatrick, Timothy J.; Davidson, Christina; Fletcher, Jack M.; Townsend, Irene; Tyerman, Gayle H.; Shimmin, Lawrence C.; Northrup, Hope

Founder Effect of the 669insA Mutation in BSCL2 Gene Causing Berardinelli-Seip Congenital Lipodystrophy in a Cluster from Brazil
pp. 729-734(6)
Authors: Gomes, K. B.; Pardini, V. C.; Ferreira, A. C. S.; Fonseca, C. G.; Fernandes, A. P.

Sex-Specific Effects of AGT-6 and ACE I/D on Pulse Pressure After 6 Months on Antihypertensive Treatment: The GenHAT Study
pp. 735-745(11)
Authors: Lynch, A. I.; Arnett, D. K.; Davis, B. R.; Boerwinkle, E.; Ford, C. E.; Eckfeldt, J. H.; Leiendecker-Foster, C.

Evaluation of the Thyroid Transcription Factor-1 Gene (TITF1) as a Hirschsprung's Disease Locus
pp. 746-754(9)
Authors: Garcia-Barceló, Maria-Mercè; Lau, Danny Ko-chun; Ngan, Elly Sau-wai; Leon, Thomas Yuk-yu; Liu, Ting-ting; So, Man-ting; Miao, Xiao-ping; Lui, Vincent Chi-hang; Wong, Kenneth Kak-yuen; Ganster, Raymond William; Cass, Daniel Thomas; Croaker, Geoffrey David Hain; Tam, Paul Kwong-hang

Persistence of the Common Hartnup Disease D173 N Allele in Populations of European Origin
pp. 755-761(7)
Authors: Azmanov, Dimitar N.; Rodgers, Helen; Auray-Blais, Christiane; Giguère, Robert; Bailey, Charles; Bröer, Stefan; Rasko, John E. J.; Cavanaugh, Juleen A.

Variation in 5' Promoter Region of the APOE gene Contributes to Predicting Ischemic Heart Disease (IHD) in the Population at Large: the Copenhagen City Heart Study
pp. 762-771(10)
Authors: Stengård, J. H.; Frikke-Schmidt, R.; Tybjærg-Hansen, A.; Nordestgaard, B.G.; Sing, C.F.

Association of Microsatellite Polymorphisms of the Human 14q13.2 Region with Type 2 Diabetes Mellitus in Latvian and Finnish Populations
pp. 772-776(5)
Authors: Sjakste, T.; Kalis, M.; Poudziunas, I.; Pirags, V.; Lazdins, M.; Groop, L.; Sjakste, N.

No Association of the ACTN3 Gene R577X Polymorphism with Endurance Performance in Ironman Triathlons
pp. 777-781(5)
Authors: Saunders, C. J.; September, A. V.; Xenophontos, S. L.; Cariolou, M. A.; Anastassiades, L. C.; Noakes, T. D.; Collins, M.

Mitochondrial and Y Chromosome Diversity in the English-Speaking Caribbean
pp. 782-790(9)
Authors: Torres, J. Benn; Kittles, R. A.; Stone, A. C.

Migration Rates and Genetic Structure of two Hungarian Ethnic Groups in Transylvania, Romania
pp. 791-803(13)
Authors: Brandstätter, A.; Egyed, B.; Zimmermann, B.; Duftner, N.; Padar, Z.; Parson, W.

A Novel Approach to Detect Parent-of-Origin Effects from Pedigree Data with Application to Beckwith-Wiedemann Syndrome
pp. 804-814(11)
Authors: Shete, Sanjay; Elston, Robert C.; Lu, Yue

Fine Mapping of Disease Genes Using Tagging SNPs
pp. 815-827(13)
Authors: Sjölander, Arvid; Hössjer, Ola; Hartman, Linda Werner; Humphreys, Keith

Sample Size Needed to Detect Gene-Gene Interactions Using Linkage Analysis
pp. 828-842(15)
Authors: Wang, Shuang; Zhao, Hongyu

Interleukin 6 Variable Number of Tandem Repeats (VNTR) Gene Polymorphism in Centenarians
pp. 843-848(6)
Authors: Capurso, C.; Solfrizzi, V.; D'Introno, A.; Colacicco, A. M.; Capurso, S. A.; Semeraro, C.; Capurso, A.; Panza, F.