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R Straussberg

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

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Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 22, 2013
A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab-Israeli familyM Abu-Rashid, M Mahajnah, L Jaber, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, et al.
Journal of Medical Genetics|July 22, 2005
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.
Neurology|January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizuresR Straussberg, L Basel-Vanagaite, S Kivity, et al.
Molecular Genetics and Metabolism|October 3, 2002
Seventeen novel mutations that cause profound biotinidase deficiencyB Wolf, K Jensen, G Hüner, 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.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 22, 2013
A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab-Israeli familyM Abu-Rashid, M Mahajnah, L Jaber, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, et al.
Journal of Medical Genetics|July 22, 2005
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.
Neurology|January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizuresR Straussberg, L Basel-Vanagaite, S Kivity, et al.
Molecular Genetics and Metabolism|October 3, 2002
Seventeen novel mutations that cause profound biotinidase deficiencyB Wolf, K Jensen, G Hüner, et al.
Pageof 8