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R J Leach

Showing results (71-80 of 76) with videos related to

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Acta Psychiatrica Scandinavica|April 28, 2006
Association analyses of the neuregulin 1 gene with schizophrenia and manic psychosis in a Hispanic populationC Walss-Bass, H Raventos, A P Montero, et al.
American Journal of Medical Genetics|July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18qJ D Cody, P D Ghidoni, B R DuPont, et al.
Annals of Human Genetics|January 31, 2006
Golli-MBP copy number analysis by FISH, QMPSF and MAPH in 195 patients with hypomyelinating leukodystrophiesC Vaurs-Barriere, M-N Bonnet-Dupeyron, P Combes, et al.
Urologic Oncology|December 13, 2003
Chromosome 18 suppresses prostate cancer metastasesS S Padalecki, K S Weldon, X T Reveles, et al.
American Journal of Medical Genetics|July 25, 1997
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiencyC T Gay, L J Hardies, R A Rauch, et al.
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Pageof 8

Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Acta Psychiatrica Scandinavica|April 28, 2006
Association analyses of the neuregulin 1 gene with schizophrenia and manic psychosis in a Hispanic populationC Walss-Bass, H Raventos, A P Montero, et al.
American Journal of Medical Genetics|July 16, 1999
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18qJ D Cody, P D Ghidoni, B R DuPont, et al.
Annals of Human Genetics|January 31, 2006
Golli-MBP copy number analysis by FISH, QMPSF and MAPH in 195 patients with hypomyelinating leukodystrophiesC Vaurs-Barriere, M-N Bonnet-Dupeyron, P Combes, et al.
Urologic Oncology|December 13, 2003
Chromosome 18 suppresses prostate cancer metastasesS S Padalecki, K S Weldon, X T Reveles, et al.
American Journal of Medical Genetics|July 25, 1997
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiencyC T Gay, L J Hardies, R A Rauch, et al.
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
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