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14篇 您的检索式:作者名="Aula P"
    题名 作者 年代 出处 被引量
1A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy显示文摘Huoponen K vilkki J Aula P 1991Am J Hum Genet1991,48,6:1
2Distribution of cytoplasmic vacuoles in blood T and B lymphocytes in two lysosomal disorders 显示文摘Aula P Rapola J Andersson LC 1975Virchows Arch B Cell Pathol1975,18,4:1
3Database for the mutations of the Finnish disease heritage显示文摘Sipila K Aula P 2002Hum Mutat2002,19,1:1
4Effects of feedback and dwell time on eye typing speed and accuracy 显示文摘Majaranta P MacKenzie I S Aula A 2006Journal of Universal Access in the Information Society2006,5,2:1
5Social Media, Reputation Risk and Ambient Publicity Man- agement 显示文摘Aula P 2010Strategy & Leadership2010,,6:1
6A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy显示文摘Huoponen K Vilkki J Aula P 1991Am J Hum Genet1991,48,6:1
7'Salla dis- ease', a new lysosomal storage disorder 显示文摘AULA P AUTIO S RAIVIO K O 1979Arch Neu- rol1979,36,2:1
8A new mtDNA mutation associated with Leber hereditary optic neuroretionpathy显示文摘Huoponen K Vilkki J Aula P 1991Am J Hum Genet1991,48,6:1
9A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy 显示文摘Huoponen K Vilkki J Aula P 1991Am J Hum Genet1991,48,:1
10Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene显示文摘Isoniemi A Hietala M Aula P 1995Hum Mutat1995,5,:1
11Impact o f marked w eight l oss i nduced b y bariatric s urgery o n bone mineral density and remodeling显示文摘Pereira F A d e Castro J A d os Santos J E Foss MC P aula F J 0,,:1
12The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy显示文摘 Lamminen T Juvonen V Aula P Nikoskelainen E Savontaus ML 1993Hum Genet1993,92,:1
13Spectrum of mutations in aspartylglucosaminuria显示文摘Ikonen E Aula P Gr(o)n K 1991Proc Natl Acad Sci USA1991,88,11:1
14A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy 显示文摘Huoponen K Vilkki J Aula P 1991Am J HumGenet1991,48,:1
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