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Kati Donner yritystiedot | Y-tunnus | Kauppalehti
www.kauppalehti.fi
Kauppalehden Yrityshausta saat helposti yrityksen yhteystiedot, kaupparekisteriotteen, yrityksen maksuhäiriömerkinnät, yhtiöjärjestyksen, vastuuhenkilöt sekä...
Weston County Gazette December 4, 2003: Page 6
wcg.stparchive.com
Weston County Gazette Newspaper Archive Upton Wyoming; December Page 6. Topics include upton, love, tree, twin, offered, team, spruce, kristi, grade,...
Weston County Gazette October 16, 2003: Page 7
wcg.stparchive.com
Weston County Gazette Newspaper Archive Upton Wyoming; October Page 7. Topics include upton, students, school, jessica, act, test, grade, games, win,...
Telephone & Addresses
Kati Donner, Gillette, US, S Brooks Ave
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Business Profiles
Researchgate: Kati Donner
Helsinki, Finland
Bad news
findagrave: Donner, Katie Irene Harwick
, Green (Summit County, Ohio)
findagrave: Donner, Katie Myer
, Jennings (St. Louis County, Missouri)
Books & Literature
Roles of the Nebulin and [beta]-tropomyosin Genes in Nemaline...
books.google.de
Kati Donner, pages. 0 Reviewshttp://books.google.com/books/about/Roles_of_the_Nebulin_and_beta_tropomyosi.html?id=95Z5JwAACAAJ ...
Related Documents
CiteSeerX — and
citeseerx.ist.psu.edu
by Kati Donner , Docent Carina Wallgren-pettersson , Ph. D , Docent Katarina Pelin , Ph. D , Professor Olli Carpén , Ph. D , Docent Kirsi Huoponen ...
Abnormal actin binding of aberrant β-tropomyosins is a molecular...
portlandpress.com
Minttu MARTTILA*†, Elina LEMOLA*†, William WALLEFELD‡, Massimiliano MEMO§, Kati DONNER, Nigel G. LAING‡,. Steven MARSTON§, Mikaela GR ...
Contents, Human Mutation | humu | DeepDyve
www.deepdyve.com
OFFICIAL JOURNAL Human Mutation Variation, Informatics, and Disease www.hgvs.org Volume 35, Number 12, December FEATURES v In This Issue REVIEWS page
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of...
www.scienceopen.com
Nemaline myopathy is a clinically and genetically heterogeneous muscle disorder. In the nebulin gene we have detected a number of autosomal...
Publications
Genetic Loci Associated with Allergic Sensitization in Lithuanians -...
core.ac.uk
By Ingrida Sauliene, Jurate Greiciuviene, Laura Sukiene, Neringa Juskeviciute, Christian Benner, Aukse Zinkeviciene, Samuli Ripatti, Kati Donner and Denis ...
Laboratory tests as predictors of the antihypertensive effects of...
www.biomedsearch.com
OBJECTIVE: Individual blood pressure responses to antihypertensive therapy are difficult to predict. To improve optimization of antihypertensive therapy, we...
Kati Donner's Research on Tropomyosin | CureHunter
www.curehunter.com
, Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. Join CureHunter, for free Research Interface BASIC access!
Miscellaneous
Kati Donner, Veikkola | NetInfo
www.netinfo.fi
Kati Donner. Osoite, Kullervonkuja Veikkola. Puhelin. Toimiala, Siivous. Kirjaudu sisään · Info · Palaute · Lisää tiedot · Autohuolto · Pitopalvelu ...
Anxiety Disorders: Donner, Kati - Expertscape.com
www.expertscape.com
Kati Donner has special expertise in Anxiety Disorders
DONNER ULLA KATARINA | Yrityksen yhteystiedot - Hakemistokeskus.fi
kirkkonummi.hakemistokeskus.fi
Hakemistokeskus.fi - Yrityshakemisto - Toimialahakemisto
Kati M. Donner — University of Helsinki
researchportal.helsinki.fi
ID: Institute for Molecular Medicine Finland (FIMM). PL 20 (Tukholmankatu 8). Building: F213b. HELSINGIN YLIOPISTO. Finland. .
Clinical and genetic heterogeneity in autosomal recessive nemaline...
www.infona.pl
Kati Donner. Department of Medical Genetics, University of Helsinki, and The Folkhälsan Institute of Genetics, Helsinki, Finland Department of Clin… see all ...
Clinical and genetic heterogeneity in autosomal recessive nemaline...
utsouthwestern.pure.elsevier.com
Carina Wallgren-Pettersson, Katarina Pelin, Pirta Hilpelä, Kati Donner, Berardino Porfirio, Claudio Graziano, Kathryn J. Swoboda, Michel ...
(PDF) C.P One causative gene, TPM2, and two congenital...
www.academia.edu
C.P One causative gene, TPM2, and two congenital myopathies. A functional study
(PDF) Clinical and genetic heterogeneity in autosomal recessive...
www.academia.edu
By Kati Donner and Roberto Cusano in Genetics and Humans.
CRY2 Genetic Variants Associate with Dysthymia (pdf) | Paperity
paperity.org
Paperity: the 1st multidisciplinary aggregator of Open Access journals & papers. Free fulltext PDF articles from hundreds of disciplines, all in one place
Chih-Chung Liu, Li-Jen Su, Wei-Yuan Tsai, Hsiao-Lun Sun, Hoong ...
www.jcircadianrhythms.com
DOI: http://www.dx.doi.org hr ; Leena Kovanen, Kati Donner, Mari Kaunisto, Timo Partonen "CRY1, CRY2 and PRKCDBP genetic ...
CRY2 Genetic Variants Associate with Dysthymia
journals.plos.org
Kati Donner,. Affiliation: Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland. X. Sirkku T. Saarikoski,.
FIMM Technology Services FIMM:n teknologiapalvelut 1 - PDF Ilmainen...
docplayer.fi
Sequencing services: Pekka Ellonen () + Genotyping services: Kati Donner () +
GENRES: GENes and Antihypertensive Drug RESponse » ICAPS
icaps-htn.org
Kimmo Kontula, University of Helsinki, Principal Investigator; Timo Hiltunen, University of Helsinki; Kati Donner, University of Helsinki ...
Katarina Pelin
www.infona.pl
Carina Wallgren-Pettersson, Kati Donner, Caroline Sewry, Emilia Bijlsma, more · Neuromuscular Disorders 12 , 7-8 ,
(PDF) Mutations in the skeletal muscle α-actin gene in patients with...
www.academia.edu
Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy. Authors. Katarina Pelin + 4. Katarina Pelin. Kati Donner.
Malijet Modibo Sidibé et Soumana Sako veulent créer un pôle politique...
malijet.com
Modibo Sidibé et Soumana Sako veulent créer un pôle politique de la Gauche républicaine, démocratique et sociale
SpringerCitations - Details Page
citations.springernature.com
Vilma-Lotta Lehtokari, Kirsi Kiiski, Sarah A. Sandaradura, Jocelyn Laporte, Pauliina Repo, Jennifer A. Frey, Kati Donner, Minttu Marttila, Carol Saunders, Peter ...
Genetic Loci Associated with Allergic Sensitization in Lithuanians
figshare.com
Genetic Loci Associated with Allergic Sensitization in Lithuanians
SIRT1 Polymorphisms Associate with Seasonal Weight Variation,...
journals.plos.org
Kati Donner,. Affiliation Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland. ⨯. Timo Partonen. Affiliation ...
Ta tillvara på äpplen! - Julia K - Metro Mode
juliak.metromode.se
Godmorgon raringar! Just lämnat av barnen. På deras respektive skolor. Tre olika
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