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المؤلفون: Sanjana Ratakonda, Davis P. Argersinger, Gabriella C. Auchus, Caroline McGowan, Hannah Ship, David R. Wang, Michael M. McKee
المصدر: Trends in Molecular Medicine. 28:1012-1015
مصطلحات موضوعية: Education, Medical, Humans, Molecular Medicine, Disabled Persons, Curriculum, Delivery of Health Care, Molecular Biology, Schools, Medical
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المصدر: American Journal of Medical Genetics Part A. 185:528-533
مصطلحات موضوعية: 0301 basic medicine, Pediatrics, medicine.medical_specialty, endocrine system diseases, Wolfram syndrome, Hearing loss, business.industry, nutritional and metabolic diseases, 030105 genetics & heredity, medicine.disease, eye diseases, 03 medical and health sciences, 030104 developmental biology, Cataracts, Diabetes insipidus, otorhinolaryngologic diseases, Genetics, medicine, Congenital cataracts, Sensorineural hearing loss, Allele, medicine.symptom, business, Genetics (clinical), Aunt
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المؤلفون: Ashley Cannon, Heather B. Radtke, Allison L. Goetsch, Caroline McGowan, Amanda L. Bergner, Karin Panzer
المصدر: Journal of Genetic Counseling. 29:692-714
مصطلحات موضوعية: Neurofibromatosis 2, medicine.medical_specialty, Neurofibromatosis 1, Skin Neoplasms, Neurofibromatoses, medicine.diagnostic_test, Health professionals, business.industry, Genetic counseling, Genetic Counseling, medicine.disease, Resource (project management), Family medicine, medicine, Clinical genetic, Humans, Neurofibromatosis type 2, Neurofibromatosis, business, Schwannomatosis, Neurilemmoma, Societies, Medical, Genetics (clinical), Genetic testing
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المؤلفون: Yiping, Shen, Kira A, Dies, Ingrid A, Holm, Carolyn, Bridgemohan, Magdi M, Sobeih, Elizabeth B, Caronna, Karen J, Miller, Jean A, Frazier, Iris, Silverstein, Jonathan, Picker, Laura, Weissman, Peter, Raffalli, Shafali, Jeste, Laurie A, Demmer, Heather K, Peters, Stephanie J, Brewster, Sara J, Kowalczyk, Beth, Rosen-Sheidley, Caroline, McGowan, Andrew W, Duda, Sharyn A, Lincoln, Kathryn R, Lowe, Alison, Schonwald, Michael, Robbins, Fuki, Hisama, Robert, Wolff, Ronald, Becker, Ramzi, Nasir, David K, Urion, Jeff M, Milunsky, Leonard, Rappaport, James F, Gusella, Christopher A, Walsh, Bai-Lin, Wu, David T, Miller, Ludwig, von Hahn
المصدر: Pediatrics. 125(4)
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Microarray, Adolescent, Marker chromosome, Article, Cohort Studies, Young Adult, Internal medicine, Gene duplication, medicine, Humans, Genetic Testing, Child, Genetic testing, medicine.diagnostic_test, business.industry, Chromosome, Infant, Karyotype, medicine.disease, Microarray Analysis, Confidence interval, Child Development Disorders, Pervasive, Child, Preschool, Karyotyping, Pediatrics, Perinatology and Child Health, Autism, Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cad6e0eb3b8ab6303ba6e17b66cb3489
https://pubmed.ncbi.nlm.nih.gov/20231187 -
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المؤلفون: Caroline McGowan, Elizabeth Repass, Leslie Cohen, Ruthann B. Pfau, Tabitha A. Harrison, Trish Brown, Debra Lochner Doyle
المصدر: Journal of genetic counseling. 19(1)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, business.industry, Genetic counseling, Public health, MEDLINE, Survey tool, Genetic Counseling, Middle Aged, Human genetics, United States, Young Adult, Family medicine, Surveys and Questionnaires, Insurance, Health, Reimbursement, medicine, Genetics, Medical genetics, Humans, The Internet, Female, business, Genetics (clinical), Reimbursement