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S J Hayflick

Showing results (21-30 of 26) with videos related to

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Nature Genetics|December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13T D Taylor, M Litt, P Kramer, et al.
Prenatal Diagnosis|March 17, 2000
Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villiL M Linck, S J Hayflick, D S Lin, et al.
Molecular Genetics and Metabolism|April 22, 2014
PLA2G6-associated neurodegeneration (PLAN): further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset diseaseM A Illingworth, E Meyer, W K Chong, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mappingZ Kibar, M P Dubé, J Powell, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Brain : a Journal of Neurology|March 9, 2010
Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulationL Timmermann, K A M Pauls, K Wieland, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Nature Genetics|December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13T D Taylor, M Litt, P Kramer, et al.
Prenatal Diagnosis|March 17, 2000
Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villiL M Linck, S J Hayflick, D S Lin, et al.
Molecular Genetics and Metabolism|April 22, 2014
PLA2G6-associated neurodegeneration (PLAN): further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset diseaseM A Illingworth, E Meyer, W K Chong, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mappingZ Kibar, M P Dubé, J Powell, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Brain : a Journal of Neurology|March 9, 2010
Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulationL Timmermann, K A M Pauls, K Wieland, et al.
Pageof 3