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Human Genetics|July 4, 2012
Personalized medicine using DNA biomarkers: a reviewAndreas Ziegler, Armin Koch, Katja Krockenberger, et al.
Human Genetics|July 24, 2012
Heritability in the genome-wide association eraNoah Zaitlen, Peter Kraft
Human Genetics|August 14, 1998
The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A gamma-158C-->T] results from two independent gene conversion eventsG P Patrinos, P Kollia, A Loutradi-Anagnostou, et al.
Human Genetics|August 14, 1998
Microsatellite profiles reveal an unexpected genetic relationship between Asian populationsB Rolf, B Horst, A Eigel, et al.
Human Genetics|August 14, 1998
Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysisS Munné, J Fung, M J Cassel, et al.
Human Genetics|August 14, 1998
Multiple testing in fetal gender determination from maternal blood by polymerase chain reactionF Lagona, M Smid, N Papasergio, et al.
Human Genetics|September 16, 1998
Histone H4 acetylation analyses in patients with polysomy X: implications for the mechanism of X inactivationC A Leal, M L Ayala-Madrigal, L E Figuera, et al.
Human Genetics|September 16, 1998
Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22J Fischer, J A Urtizberea, S Pavek, et al.
Human Genetics|September 16, 1998
A missense Glu298Asp variant in the endothelial nitric oxide synthase gene is associated with coronary spasm in the JapaneseM Yoshimura, H Yasue, M Nakayama, et al.
Human Genetics|September 16, 1998
Molecular and clinical study of 183 patients with conotruncal anomaly face syndromeR Matsuoka, M Kimura, P J Scambler, et al.
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