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American Journal of Medical Genetics
|
January 30, 1995
Germline mosaicism at the fragile X locus
T W Prior, A C Papp, P J Snyder, et al.
Translational Psychiatry
|
January 24, 2013
Dopamine transporter DAT and receptor DRD2 variants affect risk of lethal cocaine abuse: a gene-gene-environment interaction
D Sullivan, J K Pinsonneault, A C Papp, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
September 24, 2013
Gold intercalation of boron-doped graphene on Ni(111): XPS and DFT study
W Zhao, J Gebhardt, K Gotterbarm, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
December 15, 2010
Intronic polymorphisms affecting alternative splicing of human dopamine D2 receptor are associated with cocaine abuse
Robert A Moyer, Danxin Wang, Audrey C Papp, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
January 1, 1993
Evaluation of celiac disease biopsies for adenovirus 12 DNA using a multiplex polymerase chain reaction
C J Vesy, J K Greenson, A C Papp, et al.
The Journal of Chemical Physics
|
August 21, 2009
Interaction between silver nanowires and CO on a stepped platinum surface
R Streber, B Tränkenschuh, J Schöck, et al.
BMC Bioinformatics
|
July 23, 2008
Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis
Angela P Presson, Eric M Sobel, Paivi Pajukanta, et al.
Genetic Epidemiology
|
July 6, 2016
Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women
Su Yon Jung, Eric M Sobel, Jeanette C Papp, et al.
Orvosi Hetilap
|
February 26, 1995
[Screening for congenital anomalies in mid-term pregnancy. Prospective epidemiologic study. Fetal trisomy]
E Tóth-Pál, J Oroszné Nagy, C Papp, et al.
Journal of Inherited Metabolic Disease
|
December 25, 2008
A novel mutation in NDUFS4 causes Leigh syndrome in an Ashkenazi Jewish family
S L Anderson, W K Chung, J Frezzo, et al.
Page
of 23
Search research articles
Search
Showing results (151-160 of 227) with videos related to
Sort By:
Page
of 23
American Journal of Medical Genetics
|
January 30, 1995
Germline mosaicism at the fragile X locus
T W Prior, A C Papp, P J Snyder, et al.
Translational Psychiatry
|
January 24, 2013
Dopamine transporter DAT and receptor DRD2 variants affect risk of lethal cocaine abuse: a gene-gene-environment interaction
D Sullivan, J K Pinsonneault, A C Papp, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
September 24, 2013
Gold intercalation of boron-doped graphene on Ni(111): XPS and DFT study
W Zhao, J Gebhardt, K Gotterbarm, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
December 15, 2010
Intronic polymorphisms affecting alternative splicing of human dopamine D2 receptor are associated with cocaine abuse
Robert A Moyer, Danxin Wang, Audrey C Papp, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
January 1, 1993
Evaluation of celiac disease biopsies for adenovirus 12 DNA using a multiplex polymerase chain reaction
C J Vesy, J K Greenson, A C Papp, et al.
The Journal of Chemical Physics
|
August 21, 2009
Interaction between silver nanowires and CO on a stepped platinum surface
R Streber, B Tränkenschuh, J Schöck, et al.
BMC Bioinformatics
|
July 23, 2008
Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis
Angela P Presson, Eric M Sobel, Paivi Pajukanta, et al.
Genetic Epidemiology
|
July 6, 2016
Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women
Su Yon Jung, Eric M Sobel, Jeanette C Papp, et al.
Orvosi Hetilap
|
February 26, 1995
[Screening for congenital anomalies in mid-term pregnancy. Prospective epidemiologic study. Fetal trisomy]
E Tóth-Pál, J Oroszné Nagy, C Papp, et al.
Journal of Inherited Metabolic Disease
|
December 25, 2008
A novel mutation in NDUFS4 causes Leigh syndrome in an Ashkenazi Jewish family
S L Anderson, W K Chung, J Frezzo, et al.
Page
of 23