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P Propping

Showing results (151-160 of 270) with videos related to

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Journal of Medical Genetics|February 4, 2005
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposisS Aretz, D Stienen, S Uhlhaas, et al.
Lancet (London, England)|September 30, 1995
Genetic variation of the 5-HT2A receptor and response to clozapineM M Nöthen, M Rietschel, J Erdmann, et al.
Molecular Psychiatry|July 8, 1999
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteersE G Jönsson, M M Nöthen, F Grünhage, et al.
The British Journal of Psychiatry : the Journal of Mental Science|July 1, 1993
Familial cosegregation of affective disorder and Hailey-Hailey diseaseJ Körner, M Rietschel, M M Nöthen, et al.
American Journal of Medical Genetics|November 22, 1996
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disordersG Stöber, M M Nöthen, P Pörzgen, et al.
Psychiatric Genetics|January 1, 1996
Apolipoprotein E genotype distribution in schizophreniaS Zhu, M M Nöthen, S Uhlhaas, et al.
Acta Psychiatrica Scandinavica|November 1, 1995
Clinical evidence for genomic imprinting in bipolar I disorderM Grigoroiu-Serbanescu, M Nothen, P Propping, et al.
The American Journal of Dermatopathology|October 27, 1999
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic studyA Rütten, W Burgdorf, H Hügel, et al.
The Journal of Pathology|November 2, 2007
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndromeN Rahner, N Friedrichs, V Steinke, et al.
American Journal of Medical Genetics|January 23, 2002
Different familial transmission patterns in bipolar I disorder with onset before and after age 25M Grigoroiu-Serbanescu, M Martinez, M M Nöthen, et al.
Pageof 27

Showing results (151-160 of 270) with videos related to

Sort By:
Pageof 27
Journal of Medical Genetics|February 4, 2005
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposisS Aretz, D Stienen, S Uhlhaas, et al.
Lancet (London, England)|September 30, 1995
Genetic variation of the 5-HT2A receptor and response to clozapineM M Nöthen, M Rietschel, J Erdmann, et al.
Molecular Psychiatry|July 8, 1999
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteersE G Jönsson, M M Nöthen, F Grünhage, et al.
The British Journal of Psychiatry : the Journal of Mental Science|July 1, 1993
Familial cosegregation of affective disorder and Hailey-Hailey diseaseJ Körner, M Rietschel, M M Nöthen, et al.
American Journal of Medical Genetics|November 22, 1996
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disordersG Stöber, M M Nöthen, P Pörzgen, et al.
Psychiatric Genetics|January 1, 1996
Apolipoprotein E genotype distribution in schizophreniaS Zhu, M M Nöthen, S Uhlhaas, et al.
Acta Psychiatrica Scandinavica|November 1, 1995
Clinical evidence for genomic imprinting in bipolar I disorderM Grigoroiu-Serbanescu, M Nothen, P Propping, et al.
The American Journal of Dermatopathology|October 27, 1999
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic studyA Rütten, W Burgdorf, H Hügel, et al.
The Journal of Pathology|November 2, 2007
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndromeN Rahner, N Friedrichs, V Steinke, et al.
American Journal of Medical Genetics|January 23, 2002
Different familial transmission patterns in bipolar I disorder with onset before and after age 25M Grigoroiu-Serbanescu, M Martinez, M M Nöthen, et al.
Pageof 27