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B Wirth

Showing results (91-100 of 119) with videos related to

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Genomics|September 16, 1999
Comparative sequence analysis of the mouse and human Lgn1/SMA intervalM Endrizzi, S Huang, J M Scharf, et al.
Journal of Child Neurology|August 13, 1998
Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophyH Omran, U P Ketelsen, F Heinen, et al.
Harvard Review of Psychiatry|April 25, 2007
Head banging on an inpatient psychiatric unit: a vicious circleJessica E Daniels, James B Wirth, Daniel G Herrera, et al.
Journal of Medical Genetics|July 30, 2008
Congenital heart disease is a feature of severe infantile spinal muscular atrophyS Rudnik-Schöneborn, R Heller, C Berg, et al.
Clinical Genetics|September 29, 2009
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counsellingS Rudnik-Schöneborn, C Berg, K Zerres, et al.
Contributions to Nephrology|January 1, 1992
The molecular genetics of autosomal-dominant polycystic kidney disease of the PKD1 typeS Somlo, G G Germino, B Wirth, et al.
Human Molecular Genetics|August 1, 1995
Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAsB Wirth, E Hahnen, K Morgan, et al.
Genomics|March 1, 1994
Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3B Wirth, E Pick, A Leutner, et al.
The American Journal of Psychiatry|December 1, 1989
A chart review study of late-onset and early-onset schizophreniaG D Pearlson, L Kreger, P V Rabins, et al.
Nature Genetics|May 20, 1998
SMN oligomerization defect correlates with spinal muscular atrophy severityC L Lorson, J Strasswimmer, J M Yao, et al.
Pageof 12

Showing results (91-100 of 119) with videos related to

Sort By:
Pageof 12
Genomics|September 16, 1999
Comparative sequence analysis of the mouse and human Lgn1/SMA intervalM Endrizzi, S Huang, J M Scharf, et al.
Journal of Child Neurology|August 13, 1998
Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophyH Omran, U P Ketelsen, F Heinen, et al.
Harvard Review of Psychiatry|April 25, 2007
Head banging on an inpatient psychiatric unit: a vicious circleJessica E Daniels, James B Wirth, Daniel G Herrera, et al.
Journal of Medical Genetics|July 30, 2008
Congenital heart disease is a feature of severe infantile spinal muscular atrophyS Rudnik-Schöneborn, R Heller, C Berg, et al.
Clinical Genetics|September 29, 2009
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counsellingS Rudnik-Schöneborn, C Berg, K Zerres, et al.
Contributions to Nephrology|January 1, 1992
The molecular genetics of autosomal-dominant polycystic kidney disease of the PKD1 typeS Somlo, G G Germino, B Wirth, et al.
Human Molecular Genetics|August 1, 1995
Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAsB Wirth, E Hahnen, K Morgan, et al.
Genomics|March 1, 1994
Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3B Wirth, E Pick, A Leutner, et al.
The American Journal of Psychiatry|December 1, 1989
A chart review study of late-onset and early-onset schizophreniaG D Pearlson, L Kreger, P V Rabins, et al.
Nature Genetics|May 20, 1998
SMN oligomerization defect correlates with spinal muscular atrophy severityC L Lorson, J Strasswimmer, J M Yao, et al.
Pageof 12