-
1
المؤلفون: J. E. Heine, D. L. Van Dyke, J. N. Devlin
المصدر: IEEE Aerospace and Electronic Systems Magazine. 27:8-15
مصطلحات موضوعية: Continuous-wave radar, Bistatic radar, Radar engineering details, Space and Planetary Science, Computer science, Pulse-Doppler radar, Radar imaging, Aerospace Engineering, Fire-control radar, Electrical and Electronic Engineering, Low-frequency radar, Radar horizon, Remote sensing
-
2
المؤلفون: Stephanie A. Smoley, R Fonseca, Esteban Braggio, Scott VanWier, Neil E. Kay, Renee C. Tschumper, Traci Sassoon, John C. Byrd, Michael T. Barrett, D F Jelinek, Tait D. Shanafelt, D L Van Dyke, Jeanette E. Eckel-Passow
المصدر: Leukemia. 26:1698-1701
مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, Chronic lymphocytic leukemia, Biology, Article, Evolution, Molecular, Internal medicine, medicine, Humans, Longitudinal Studies, Survival rate, In Situ Hybridization, Fluorescence, Chromosome Aberrations, Hematology, Genome, Human, Disease progression, Clonal architecture, Prognosis, medicine.disease, Leukemia, Lymphocytic, Chronic, B-Cell, Clone Cells, Lymphoma, Survival Rate, Leukemia, Oncology, Mutation, Immunology, Disease Progression, Human genome
-
3
المؤلفون: D. L. Van Dyke, Lester Weiss, V. R. Babu
المصدر: Clinical Genetics. 32:75-79
مصطلحات موضوعية: Genetics, Pediatrics, medicine.medical_specialty, Models, Genetic, Derivative chromosome, Marker chromosome, Isochromosome, Trisomy, Biology, medicine.disease, Paternal Age, Mutation, medicine, Humans, Chromosome 21, Genetics (clinical), Maternal Age
-
4
المؤلفون: Gail H. Vance, D. L. Satinover, Stuart Schwartz, D. L. Van Dyke
المصدر: Chromosoma. 110:275-283
مصطلحات موضوعية: Chromosomes, Artificial, Bacterial, Neocentromere, Centromere, Fluorescent Antibody Technique, Chromosome 9, CHO Cells, Hybrid Cells, Biology, Genome, DNA sequencing, Cricetinae, Chromosome 19, Genetics, Animals, Humans, In Situ Hybridization, Fluorescence, Genetics (clinical), DNA Primers, Chromosome Aberrations, Bacterial artificial chromosome, Base Sequence, Contig, Molecular biology, Karyotyping, Chromosomes, Human, Pair 9, Chromosome 22
-
5Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature
المؤلفون: P M Czarnecki, D. L. Van Dyke, G.L. Feldman, E.V. Bawle, J.V. Conard, Anne E. Wiktor
المصدر: Annales de Génétique. 44:129-134
مصطلحات موضوعية: Male, medicine.medical_specialty, Adolescent, Foot Deformities, Congenital, Chromosomal translocation, Biology, Translocation, Genetic, Head shape, Gene Duplication, Gene duplication, Genetics, medicine, Humans, In Situ Hybridization, Fluorescence, Nose, Family Health, Hand deformity, medicine.diagnostic_test, Chromosomes, Human, Pair 10, Cytogenetics, Facies, Infant, Karyotype, Syndrome, medicine.disease, Chromosome Banding, Pedigree, medicine.anatomical_structure, Chromosomes, Human, Pair 2, Face, Karyotyping, Female, Chromosome Deletion, Hand Deformities, Congenital, Fluorescence in situ hybridization
-
6
المؤلفون: TURNER SYNDROME STUDY G.R.O.U.P. Bondy CA, Turner Sindrome Study Group: Turner Sindrome Consensus Study Group: Neus Baena, V. K. Bakalov, B. B. Biesecker, J. C. Carel, G. Conway, M. Davenport, C. Disteche, M. F. Karnis, J. A. Germak, C. H. Gravholt, J. Foodim, D. Gunther, O. Hovatta, A. M. Kappelgard, W. Kiess, K. Landin Wilhelmsen, A. Lin, B. Lippe, M. Loscalzo, K. Lynch, M. M. M. Mazzocco, E. McCauley, P. McDonough, S. M. P. F. de Muinck Keizer Schrama, R. W. Naeraa, C. Quigley, R. Rosenfield, D. Rosing, J. Ross, D. Roulot, K. Rubin, P. Saenger, P. Schmidt, M. Silberbach, V. Sybert, D. L. Van Dyke, A. Zinn, MAZZANTI, LAURA
المساهمون: TURNER SYNDROME STUDY GROUP. Bondy CA and Turner Sindrome Study Group: Turner Sindrome Consensus Study Group: Neus Baena, V. K. Bakalov, B.B. Biesecker, J.C. Carel, G.Conway, M. Davenport, C. Disteche, M. F. Karni, J. A. Germak, C.H. Gravholt, J. Foodim, D. Gunther, O. Hovatta, A.M. Kappelgard, W. Kie, K. Landin-Wilhelmsen, A. Lin, B. Lippe, M. Loscalzo, K. Lynch, L. Mazzanti, M. M. M. Mazzocco, E. McCauley, P. McDonough, S.M.P.F. de Muinck Keizer-Schrama, R. W. Naeraa, C. Quigley, R. Rosenfield, D. Rosing, J. Ro, D. Roulot, K. Rubin, P. Saenger, P. Schmidt, M. Silberbach, V. Sybert, D. L. Van Dyke, A. Zinn.
مصطلحات موضوعية: Adult, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, media_common.quotation_subject, Clinical Biochemistry, MEDLINE, Turner Syndrome, Biochemistry, Bone and Bones, Child health, Presentation, Cognition, Neonatal Screening, Endocrinology, Multidisciplinary approach, Prenatal Diagnosis, Internal medicine, Turner syndrome, Good evidence, medicine, Humans, Child, media_common, Web site, business.industry, Liver Diseases, Estrogen Replacement Therapy, Puberty, Biochemistry (medical), Infant, Newborn, Guideline, medicine.disease, Fertility, Cardiovascular Diseases, Female, business, GROWTH-HORMONE TREATMENT, SEX-CHROMOSOME ABNORMALITIES, LERI-WEILL DYSCHONDROSTEOSIS, CARDIOVASCULAR RISK-FACTORS, CONGENITAL HEART-DISEASE, RANDOMIZED DOSE-RESPONSE, PULMONARY VENOUS RETURN, POPULATION-BASED COHORT, BONE-MINERAL DENSITY, QUALITY-OF-LIFE
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c975f3e5d31204ad3b3c737d05d8c3b0
http://hdl.handle.net/11585/124715 -
7
المؤلفون: D. L. Van Dyke, Lisa G. Shaffer, Angela Scheuerle, David H. Ledbetter, Frank Greenberg, J. L. Zenger-Hain
المصدر: American Journal of Medical Genetics. 56:403-408
مصطلحات موضوعية: Male, X Chromosome, Chromosomal translocation, Biology, Translocation, Genetic, Chromosome 15, Dicentric chromosome, medicine, Humans, Abnormalities, Multiple, Skewed X-inactivation, Genetics (clinical), X chromosome, Genetics, Chromosomes, Human, Pair 15, medicine.diagnostic_test, Mosaicism, Infant, Newborn, Karyotype, Syndrome, medicine.disease, Molecular biology, Uniparental disomy, Chromosome Banding, Pedigree, Phenotype, Karyotyping, Female, Fluorescence in situ hybridization
-
8
المؤلفون: C. G. Palmer, F. Elder, J. T. Lanman, S. Schwartz, Mark J. Pettenati, M. D. Higgins, Elisabeth A. Keitges, J. Brown, Kathleen W. Rao, F. Grass, R. R. Higgins, M. G. Butler, D. L. Van Dyke, Colleen Jackson-Cook, P. N. Rao, J. L. Smith, P. Cosper, A. J. Carroll, M. C. Phelan, F.W. Luthardt
المصدر: American Journal of Medical Genetics. 55:171-187
مصطلحات موضوعية: Recombination, Genetic, Genetics, Autosome, Offspring, Incidence, Breakpoint, Chromosome, Aneuploidy, Syndrome, Biology, medicine.disease, Congenital Abnormalities, Chromosome Inversion, Gene duplication, medicine, Humans, Genetics (clinical), Chromosomal Deletion, Chromosomal inversion
-
9
المؤلفون: A Tefferi, Mario Cazzola, Francisco Cervantes, D L Van Dyke, Kebede H. Begna, E. Morra, Naseema Gangat, Alessandro M. Vannucchi, Francesco Passamonti, C A Hanson, A. Pardanani, Domenica Caramazza, Arturo Pereira
المصدر: Leukemia. 26(6)
مصطلحات موضوعية: Oncology, Adult, Male, Cancer Research, Pediatrics, medicine.medical_specialty, Adolescent, Constitutional symptoms, Immunology, Biochemistry, Gastroenterology, Cohort Studies, Young Adult, International database, Risk Factors, Internal medicine, medicine, Humans, Myelofibrosis, Aged, Aged, 80 and over, Acute leukemia, Primary (chemistry), Leukemia, Models, Statistical, Receiver operating characteristic, business.industry, International Agencies, Primary myelofibrosis, Prognostic model, Cell Biology, Hematology, International working group, Middle Aged, medicine.disease, Survival Rate, ROC Curve, International Prognostic Scoring System, Primary Myelofibrosis, Karyotyping, Cohort, Female, business, Follow-Up Studies
-
10
المؤلفون: Animesh Pardanani, Naseema Gangat, A Tefferi, C A Hanson, Kebede H. Begna, Domenica Caramazza, Rakhee Vaidya, D L Van Dyke, Sergio Siragusa
المساهمون: Caramazza, D, Begna, K, Gangat, N, Vaidya, R, Siragusa, S, Van Dyke, D, Hanson, C, Pardanani, A, Tefferi, A
المصدر: Leukemia
مصطلحات موضوعية: Adult, Male, Risk, Cancer Research, medicine.medical_specialty, Pathology, Adolescent, Chromosomal translocation, myelofibrosis, Gastroenterology, cytogenetics, Disease-Free Survival, Settore MED/15 - Malattie Del Sangue, Internal medicine, Complex Karyotype, medicine, Humans, Myelofibrosis, Aged, Aged, 80 and over, Chromosome Aberrations, Leukemia, Hematology, Platelet Count, business.industry, Hazard ratio, Karyotype, Middle Aged, Prognosis, medicine.disease, Confidence interval, karyotype, Oncology, Primary Myelofibrosis, International Prognostic Scoring System, Karyotyping, Original Article, Female, myeloproliferative, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f30f5a1a22ac11f1be3903f9d2438c50
http://hdl.handle.net/10447/75836