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المؤلفون: Lagerström-Fermér, Maria, Sundvall, Mats, Johnsen, Elsy, Warne, GL, Forrest, SM, Zajac, JD, Richards, A, Ravine, D, Landegren, Ulf, Pettersson, Ulf
المصدر: American Journal of Human Genetics. 60(4):910-916
وصف الملف: print
URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-51918
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1712462/ -
2دورية أكاديمية
المؤلفون: Olsson, Charlotta, Johnsen, Elsy, Nilsson, Mats, Wilander, Erik, Syvänen, Ann-Christine, Lagerström-Fermér, Maria
المصدر: European Journal of Human Genetics; Dec2001, Vol. 9 Issue 12, p917, 5p
مصطلحات موضوعية: GENETIC mutation, MITOCHONDRIAL DNA, DIABETES, DEAFNESS
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3دورية أكاديمية
المؤلفون: Lagerström-Fermér M; Department of Medical Sciences, Unit of Molecular Medicine, University Hospital, Uppsala, Sweden. Maria. Lagerstrom@medsci.uu.se, Larhammar D, Johnsen E, Landegren U
المصدر: Genomics [Genomics] 2002 Mar; Vol. 79 (3), pp. 432-6.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 8800135 Publication Model: Print Cited Medium: Print ISSN: 0888-7543 (Print) Linking ISSN: 08887543 NLM ISO Abbreviation: Genomics Subsets: MEDLINE
مواضيع طبية MeSH: Genomics/*methods , Polymerase Chain Reaction/*methods, 3' Untranslated Regions/genetics ; Animals ; Base Sequence ; Humans ; Molecular Sequence Data ; Phylogeny ; Sequence Alignment ; Somatostatin/genetics
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