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1دورية أكاديمية
المؤلفون: Plenge RM; Department of Genetics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA., Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, Winter RM, Willard HF
المصدر: Nature genetics [Nat Genet] 1997 Nov; Vol. 17 (3), pp. 353-6.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Print ISSN: 1061-4036 (Print) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE
مواضيع طبية MeSH: Dosage Compensation, Genetic* , Mutation* , RNA, Untranslated*, Transcription Factors/*genetics, Deoxyribonucleases, Type II Site-Specific/genetics ; Deoxyribonucleases, Type II Site-Specific/metabolism ; Female ; Haplotypes ; Humans ; Male ; Pedigree ; Promoter Regions, Genetic ; RNA, Long Noncoding ; Receptors, Androgen/genetics
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2دورية أكاديمية
المؤلفون: Warburton PE; Department of Medical Genetics, University of Toronto, Ontario, Canada., Willard HF
المصدر: Journal of molecular biology [J Mol Biol] 1990 Nov 05; Vol. 216 (1), pp. 3-16.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 2985088R Publication Model: Print Cited Medium: Print ISSN: 0022-2836 (Print) Linking ISSN: 00222836 NLM ISO Abbreviation: J Mol Biol Subsets: MEDLINE
مواضيع طبية MeSH: Genes, Bacterial* , Mutation* , Operon*, Escherichia coli/*genetics , RNA, Transfer, Phe/*genetics, Amino Acid Sequence ; Base Sequence ; Molecular Sequence Data ; Plasmids ; Prephenate Dehydratase/genetics ; Prephenate Dehydratase/metabolism ; Protein Sorting Signals/genetics ; beta-Galactosidase/genetics ; beta-Galactosidase/metabolism
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3دورية أكاديمية
المؤلفون: Ingle C, Williamson R, de la Chapelle A, Herva RR, Haapala K, Bates G, Willard HF, Pearson P, Davies KE
المصدر: American journal of human genetics [Am J Hum Genet] 1985 May; Vol. 37 (3), pp. 451-62.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
مواضيع طبية MeSH: Chromosome Deletion* , Chromosome Mapping* , Mutation* , X Chromosome*, Muscular Dystrophies/*genetics, Animals ; Chromosome Banding ; Cricetinae ; Cricetulus ; DNA/genetics ; DNA Restriction Enzymes ; Female ; Genetic Linkage ; Genetic Markers ; Humans ; Hybrid Cells ; Karyotyping
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4دورية أكاديمية
المؤلفون: Willard HF, Rosenberg LE
المصدر: The Journal of clinical investigation [J Clin Invest] 1980 Mar; Vol. 65 (3), pp. 690-8.
نوع المنشور: Journal Article; Research Support, U.S. Gov't, P.H.S.
بيانات الدورية: Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model: Print Cited Medium: Print ISSN: 0021-9738 (Print) Linking ISSN: 00219738 NLM ISO Abbreviation: J Clin Invest Subsets: MEDLINE
مواضيع طبية MeSH: Apoenzymes*/genetics , Apoproteins*/genetics , Mutation*, Fibroblasts/*metabolism , Isomerases/*deficiency , Methylmalonyl-CoA Mutase/*deficiency, Alleles ; Cell Line ; Genes, Dominant ; Heterozygote ; Humans ; Kinetics ; Methylmalonyl-CoA Mutase/genetics ; Propionates/metabolism ; Vitamin B 12/pharmacology
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5دورية أكاديمية
المؤلفون: Brown CJ; Department of Medical Genetics, University of Toronto, Canada., Powers VE, Munroe DL, Sheinin R, Willard HF
المصدر: Somatic cell and molecular genetics [Somat Cell Mol Genet] 1989 Mar; Vol. 15 (2), pp. 173-8.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 8403568 Publication Model: Print Cited Medium: Print ISSN: 0740-7750 (Print) Linking ISSN: 07407750 NLM ISO Abbreviation: Somat Cell Mol Genet Subsets: MEDLINE
مواضيع طبية MeSH: Genetic Complementation Test* , Mutation* , X Chromosome*, DNA/*genetics, Animals ; Chromosome Mapping ; Humans ; Hybrid Cells ; Mice ; Temperature