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American Journal of Medical Genetics|July 13, 2002
Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophreniaAnnamari Tuulio-Henriksson, Jari Haukka, Timo Partonen, et al.American Journal of Medical Genetics|July 13, 2002
Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa RicaLynn E DeLisi, Andrea Mesen, Carlos Rodriguez, et al.American Journal of Medical Genetics|July 13, 2002
Meta-analysis of the association between tryptophan hydroxylase and suicidal behaviorA Lalovic, G TureckiAmerican Journal of Medical Genetics|July 13, 2002
A risk-factor model of epistatic interaction, focusing on autismMarshall B Jones, Peter SzatmariAmerican Journal of Medical Genetics|July 13, 2002
Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patientsHirofumi Maruyama, Yuishin Izumi, Hiroyuki Morino, et al.American Journal of Medical Genetics|July 13, 2002
Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?David Ng, Donald W Hadley, Cynthia J Tifft, et al.American Journal of Medical Genetics|July 13, 2002
Investigations of micro-organic brain damage (MOBD) in heterozygotes of metachromatic leukodystrophyAnna Tylki-Szymańska, Agnieszka Ługowska, Jolanta Chmielik, et al.American Journal of Medical Genetics|July 13, 2002
Unbalanced translocation (3;5)(q26.1;p14): a clinical reportMassimiliano Rossi, Pasqua Di Micco, Lucia Perone, et al.American Journal of Medical Genetics|July 13, 2002
Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex developmentGoro Sasaki, Tsutomu Ogata, Tomohiro Ishii, et al.American Journal of Medical Genetics|July 13, 2002
Kabuki syndrome: report of six Thai children and further phenotypic and genetic delineationVorasuk Shotelersuk, Rachaneekorn Punyashthiti, Sumarlee Srivuthana, et al.Pageof 854