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P Lichtner

Showing results (21-30 of 27) with videos related to

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European Journal of Human Genetics : EJHG|October 22, 1998
Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, et al.
Neurogenetics|August 26, 2006
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesE Stogmann, P Lichtner, C Baumgartner, et al.
Neurology|March 18, 2009
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizuresK Schlachter, U Gruber-Sedlmayr, E Stogmann, et al.
Journal of Medical Genetics|January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsM Sharma, J C Mueller, A Zimprich, et al.
Nature|August 10, 2000
GATA3 haplo-insufficiency causes human HDR syndromeH Van Esch, P Groenen, M A Nesbit, et al.
Journal of Medical Genetics|March 13, 2009
Replication of restless legs syndrome loci in three European populationsD Kemlink, O Polo, B Frauscher, et al.
Molecular Psychiatry|November 23, 2011
A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in DrosophilaK V Allebrandt, N Amin, B Müller-Myhsok, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
European Journal of Human Genetics : EJHG|October 22, 1998
Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, et al.
Neurogenetics|August 26, 2006
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesE Stogmann, P Lichtner, C Baumgartner, et al.
Neurology|March 18, 2009
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizuresK Schlachter, U Gruber-Sedlmayr, E Stogmann, et al.
Journal of Medical Genetics|January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsM Sharma, J C Mueller, A Zimprich, et al.
Nature|August 10, 2000
GATA3 haplo-insufficiency causes human HDR syndromeH Van Esch, P Groenen, M A Nesbit, et al.
Journal of Medical Genetics|March 13, 2009
Replication of restless legs syndrome loci in three European populationsD Kemlink, O Polo, B Frauscher, et al.
Molecular Psychiatry|November 23, 2011
A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in DrosophilaK V Allebrandt, N Amin, B Müller-Myhsok, et al.
Pageof 3