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المؤلفون: Arnold B. Hawk, T. Angeline, Richard J. Manners, Harsha A. Mokashi, Nirmala Jeyaraj, Heather A. Bentley, Gregory J. Tsongalis
المصدر: Experimental and Molecular Pathology. 79:9-13
مصطلحات موضوعية: DNA Mutational Analysis, Clinical Biochemistry, Population, Myocardial Infarction, India, Single-nucleotide polymorphism, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Pathology and Forensic Medicine, Risk Factors, Genotype, Prevalence, Humans, SNP, Allele, education, Molecular Biology, Genetics, education.field_of_study, Factor V, Reproducibility of Results, Molecular biology, SNP genotyping, biology.protein, Prothrombin, Restriction fragment length polymorphism, Polymorphism, Restriction Fragment Length
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المؤلفون: Jonathan P Park, Arnold B. Hawk, Sarah L Ladd, Pamela Ely, Walter W. Noll, Sarah A Wojiski, Neil J Weiner, T.K. Mohandas
المصدر: Cancer Genetics and Cytogenetics. 121:198-205
مصطلحات موضوعية: Male, Cancer Research, medicine.medical_specialty, Ring chromosome, Biology, Myelogenous, hemic and lymphatic diseases, Proto-Oncogenes, Genetics, medicine, Humans, Hairy cell leukemia, neoplasms, Molecular Biology, In Situ Hybridization, Fluorescence, Aged, Gene Amplification, Cytogenetics, Myeloid leukemia, Histone-Lysine N-Methyltransferase, Middle Aged, medicine.disease, Virology, DNA-Binding Proteins, Blotting, Southern, Leukemia, Leukemia, Myeloid, Karyotyping, Acute Disease, Chromosomal region, Acute myelomonocytic leukemia, Cancer research, Female, Myeloid-Lymphoid Leukemia Protein, Transcription Factors
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المؤلفون: James J. Filiano, Walter W. Noll, Alexander C. Mamourian, Arnold B. Hawk, Dorothy R. Belloni, T.K. Mohandas, John B. Moeschler, Richard A. Spellman, Jonathan P. Park
المصدر: American Journal of Medical Genetics. 82:294-300
مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Unequal crossing over, medicine.diagnostic_test, SnRNP Core Proteins, Locus (genetics), Biology, medicine.disease, Chromosome 15, Angelman syndrome, Gene duplication, medicine, Allele, Genetics (clinical), Fluorescence in situ hybridization
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b488ca095f646cfa7ec741508d0358af
https://doi.org/10.1002/(sici)1096-8628(19990212)82:4<294::aid-ajmg4>3.0.co;2-u -
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المؤلفون: Valerie H. Hani, Arnold B. Hawk, Dorothy R. Belloni, T.K. Mohandas, Walter W. Noll, Jonathan P. Park, John B. Moeschler
المصدر: American Journal of Medical Genetics. 78:134-139
مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Derivative chromosome, nutritional and metabolic diseases, Karyotype, Chromosomal translocation, Locus (genetics), Biology, medicine.disease, Uniparental disomy, Chromosome 15, Nondisjunction, Chromosome Arm, medicine, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::49a86959487bcad348dc5551e8f23696
https://doi.org/10.1002/(sici)1096-8628(19980630)78:2<134::aid-ajmg7>3.0.co;2-o -
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المؤلفون: Arnold B. Hawk, T.K. Mohandas, John B. Moeschler, Walter W. Noll
المصدر: American journal of medical genetics. 111(4)
مصطلحات موضوعية: Genetics, medicine.medical_specialty, Chromosomes, Human, Pair 15, Prader-Labhart-Willi Syndrome, Infant, Biology, medicine.disease, Phenotype, Genetic determinism, Central nervous system disease, Pathogenesis, Child, Preschool, Gene Duplication, Epidemiology, Gene duplication, Happy puppet syndrome, medicine, Humans, Abnormalities, Multiple, Genetics (clinical)