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Journal of Human Genetics|March 27, 2010
Molecular bases of metachromatic leukodystrophy in Polish patientsAgnieszka Lugowska, Rafał Płoski, Paweł Włodarski, et al.
Journal of Human Genetics|March 27, 2010
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardationShozo Honda, Koji O Orii, Junya Kobayashi, et al.
Journal of Human Genetics|August 21, 2008
Genetic interactions model among Eotaxin gene polymorphisms in asthmaJune-Hyuk Lee, Jason H Moore, Sung-Woo Park, et al.
Journal of Human Genetics|April 24, 2010
A two-stage case-control association study of the dihydropyrimidinase-like 2 gene (DPYSL2) with schizophrenia in Japanese subjectsTakayoshi Koide, Branko Aleksic, Yoshihito Ito, et al.
Journal of Human Genetics|April 24, 2010
Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean populationKyung-Won Hong, Hyun-Seok Jin, Ji-Eun Lim, et al.
Journal of Human Genetics|May 1, 2010
A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31-32 region and asthmaJeong-Hyun Kim, Hyun Sub Cheong, Byung-Lae Park, et al.
Journal of Human Genetics|May 9, 2009
Revisiting the peopling of Japan: an admixture perspectiveRita Rasteiro, Lounès Chikhi
Journal of Human Genetics|May 9, 2009
Mutations in the LMNA gene do not cause axonal CMT in Czech patientsPetra Lassuthová, Lucia Baránková, Jana Haberlová, et al.
Journal of Human Genetics|June 19, 2008
Gender bias in the multiethnic genetic composition of central ArgentinaA Salas, J C Jaime, V Álvarez-Iglesias, et al.
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