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Neuromuscular Disorders : NMD|April 17, 2007
GDAP1 mutations in Czech families with early-onset CMTL Baránková, E Vyhnálková, S Züchner, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|February 1, 1996
Radioreceptor binding profile of the atypical antipsychotic olanzapineF P Bymaster, D O Calligaro, J F Falcone, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1992
A human serotonin 1D receptor variant (5HT1D beta) encoded by an intronless gene on chromosome 6L Demchyshyn, R K Sunahara, K Miller, et al.
Casopis Lekaru Ceskych|September 28, 2004
[Nijmegen breakage syndrome in Slovakia]E Seemanová, V Pohanka, P Seeman, et al.
American Journal of Medical Genetics|December 15, 1994
Dopamine D4 receptor variant, D4GLYCINE194, in Africans, but not in Caucasians: no association with schizophreniaP Seeman, C Ulpian, G Chouinard, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1993
Serotonin receptor cDNA cloned from Lymnaea stagnalisK S Sugamori, R K Sunahara, H C Guan, et al.
Synapse (New York, N.Y.)|January 1, 1987
Human brain dopamine receptors in children and aging adultsP Seeman, N H Bzowej, H C Guan, et al.
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