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المؤلفون: Maimon M. Cohen, R. Ehrenpreis, Leslie J. Raffel, E. Lieber, Marcia F. Schwartz, A. Zaslav, M. Harris, Stuart Schwartz
المصدر: Clinical Genetics. 40:417-422
مصطلحات موضوعية: Genetic Markers, medicine.medical_specialty, Chromosome Disorders, Biology, Esterase, Translocation, Genetic, Carboxylesterase, Nondisjunction, Genetic, Gene duplication, Genetics, medicine, Humans, Abnormalities, Multiple, Lymphocytes, Cells, Cultured, Genetics (clinical), Chromosome Aberrations, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 10, Mosaicism, Hybridization probe, Breakpoint, Cytogenetics, Infant, Karyotype, Fibroblasts, medicine.disease, Molecular biology, Chromosome abnormality, Female, Esterase D, DNA Probes, Carboxylic Ester Hydrolases
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المؤلفون: Stuart Schwartz, Joann A. Boughman, Erik Roskes, Maimon M. Cohen
المصدر: Clinical Genetics. 38:198-210
مصطلحات موضوعية: Heart Defects, Congenital, medicine.medical_specialty, Heart disease, Heart malformation, Population, Chromosome Disorders, Biology, Internal medicine, Epidemiology, Gene duplication, Genetics, medicine, Humans, education, Genetics (clinical), Chromosome Aberrations, education.field_of_study, Maryland, Genetic heterogeneity, Infant, Newborn, Virginia, Chromosome, Karyotype, medicine.disease, Phenotype, Genes, Case-Control Studies, Karyotyping, District of Columbia, Cardiology
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المؤلفون: Judith A. Brown, Ronald G. Davidson, Maimon M. Cohen
المصدر: Clinical Genetics. 7:120-127
مصطلحات موضوعية: Genetics, Chromosome, Chromosomal translocation, Karyotype, Three generations, Biology, Genetics (clinical)
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المؤلفون: Maimon M. Cohen, Joel Charrow, Nancy E. Balkin
المصدر: Clinical Genetics. 23:304-307
مصطلحات موضوعية: Chromosomes, Human, 6-12 and X, Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Breakpoint, nutritional and metabolic diseases, Chromosomal translocation, Biology, Chromosome translocations, Translocation, Genetic, nervous system diseases, otorhinolaryngologic diseases, Humans, Female, Chromosome Deletion, Child, Prader-Willi Syndrome, Chromosomes, Human, 13-15, Genetics (clinical)
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المؤلفون: Gaurang Munshi, Laura Morsberger, Mary Haddadin, Constance A. Griffin, Antonie D. Kline, Anita L. Hawkins, R. Stephen Amato, Ilse Chudoba, Maimon M. Cohen
المصدر: American Journal of Medical Genetics. :124-129
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Chromosome Disorders, Chromosomal translocation, Biology, Intellectual Disability, Complex Karyotype, medicine, Humans, Abnormalities, Multiple, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosomal inversion, Chromosome Aberrations, medicine.diagnostic_test, Spectral Karyotyping, Brachydactyly, Cytogenetics, Nucleic Acid Hybridization, Karyotype, Anatomy, medicine.disease, Black or African American, Phenotype, Child, Preschool, Chromosomes, Human, Pair 6, Female, Fluorescence in situ hybridization, Comparative genomic hybridization
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35b1c1f70d288e4285eea3ec64c1c9ec
https://doi.org/10.1002/ajmg.a.30130 -
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المؤلفون: Bradley H Pollock, Andrew B. Campbell, Hal B. Jenson, Maimon M. Cohen, David R. Head, Christopher N. Frantz, Sharon B. Murphy, Charles T. Leach, Kenneth L. McClain, Shou-Jiang Gao
المصدر: American Journal of Hematology. 60:215-221
مصطلحات موضوعية: viruses, virus diseases, Hematology, Gene rearrangement, Biology, medicine.disease, Cell morphology, Virology, Virus, Lymphoma, law.invention, Lytic cycle, law, medicine, biology.protein, Malignant pleural effusion, Antibody, Polymerase chain reaction
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a19a1334a4bb437c96740bed03ebe3f2
https://doi.org/10.1002/(sici)1096-8652(199903)60:3<215::aid-ajh8>3.0.co;2-f -
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المؤلفون: Maimon M. Cohen, Marcia F. Schwartz, Daynna J. Wolff, Stuart Schwartz
المصدر: American Journal of Medical Genetics. 46:520-523
مصطلحات موضوعية: medicine.medical_specialty, Chromosome Disorders, Trisomy, Biology, Gene dosage, Gene mapping, Chromosome 18, Gene duplication, medicine, Aspartic Acid Endopeptidases, Humans, Abnormalities, Multiple, Genetics (clinical), Chromosomal inversion, Chromosome Aberrations, Genetics, Cytogenetics, Chromosome Mapping, Infant, Chromosome, Karyotype, Chromosome Banding, Chromosome Inversion, Female, Chromosomes, Human, Pair 18, DNA Probes
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المصدر: Clinics in Laboratory Medicine. 12:449-461
مصطلحات موضوعية: Genetics, Linkage (software), Gene mapping, Chromosome (genetic algorithm), Genetic linkage, Genetic counseling, Biochemistry (medical), Clinical Biochemistry, Disease, Biology, Risk assessment
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c0e988c14b653e9c5b6dfd8d8c6648c8
https://doi.org/10.1016/s0272-2712(18)30499-2 -
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المؤلفون: John S. Mattick, H. Winking, E. Petit, W.L. Neuman, Raju Kucherlapati, U. Hirning-Folz, Roger A. Schultz, Carol A. Westbrook, V.M. Chapman, Kenneth W. Harder, T. Shiomi, Roy Layfield, D. Benova, Howard P. Levy, Frank R. Jirik, Yoichi Matsuda, Maimon M. Cohen, Bernard H. Brownstein, Ian W. Craig, I.G. Melhado, Alessandra M.V. Duncan, Wendy Stock, Settara C. Chandrasekharappa, Robert M. Gemmill, Peter F. Nixon, M M Le Beau, Bernard Dutrillaux, M. Koleva, Y.-N. Harada, W. L. Neuman, N. Lemieux, Hélène Hayes, Christiane Löffler, G.R. Sutherland, Robert Williamson, Kyeryoung Lee, M. Abedinia, J. Battey, S. Natsuume-Sakai, L.L. Anderson, David F. Callen, Elizabeth Baker, V.V.N. Gopal Rao, Horst Hameister, N.M. Lapsys, Ingo Hansmann
المصدر: Cytogenetic and Genome Research. 61:I-IV
مصطلحات موضوعية: Botany, Genetics, Zoology, Biology, Molecular Biology, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c6d9556490bd6301fb96f164ba4b384e
https://doi.org/10.1159/000133414 -
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المؤلفون: Joann A. Boughman, S.S. Wasserman, Stuart Schwartz, Jacqueline A. Astemborski, A.P. Budacz, Maimon M. Cohen
المصدر: Mutation Research/Environmental Mutagenesis and Related Subjects. 234:51-59
مصطلحات موضوعية: Genetics, Mitomycin, Sister chromatid exchange, Biology, Toxicology, Molecular biology, 4-Nitroquinoline-1-oxide, Mitomycins, Bleomycin, Clastogen, chemistry.chemical_compound, Streptonigrin, chemistry, Reference Values, Humans, Lymphocytes, Sister Chromatid Exchange, Mutagens