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M Batbayli

Showing results (1-10 of 5) with videos related to

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Journal of Medical Genetics|September 1, 2010
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophyE Ostergaard, M Batbayli, M Duno, et al.
Clinical Genetics|August 8, 2009
Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohortS G Lindquist, M Schwartz, M Batbayli, et al.
European Journal of Neurology|February 21, 2008
Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutationS G Lindquist, I E Holm, M Schwartz, et al.
Clinical Genetics|June 2, 2012
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion diseaseS G Lindquist, M Duno, M Batbayli, et al.
European Journal of Neurology|August 30, 2008
A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairmentS G Lindquist, L Hasholt, J M C Bahl, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of Medical Genetics|September 1, 2010
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophyE Ostergaard, M Batbayli, M Duno, et al.
Clinical Genetics|August 8, 2009
Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohortS G Lindquist, M Schwartz, M Batbayli, et al.
European Journal of Neurology|February 21, 2008
Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutationS G Lindquist, I E Holm, M Schwartz, et al.
Clinical Genetics|June 2, 2012
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion diseaseS G Lindquist, M Duno, M Batbayli, et al.
European Journal of Neurology|August 30, 2008
A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairmentS G Lindquist, L Hasholt, J M C Bahl, et al.
Pageof 1