المؤلفون: Mahmoud, Ranim, Swanson, Heidi D, Butler, Merlin G, Flodman, Pamela, Gold, June-Anne, Miller, Jennifer L, Roof, Elizabeth, Osann, Kathryn, Dykens, Elisabeth, Driscoll, Daniel J, Kimonis, Virginia

المصدر: Journal of Clinical Medicine. 11(9)

مصطلحات موضوعية: Paediatrics, Biomedical and Clinical Sciences, Behavioral and Social Science, Violence Research, Brain Disorders, Pediatric, Clinical Research, Mental Health, Basic Behavioral and Social Science, Obesity, Rare Diseases, Prader-Willi syndrome, behavior, genetic subtypes, growth hormone, Prader–Willi syndrome, Clinical Sciences, Biomedical and clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/1s27w3bwTest

المؤلفون: Veatch, Olivia J, Malow, Beth A, Lee, Hye-Seung, Knight, Aryn, Barrish, Judy O, Neul, Jeffrey L, Lane, Jane B, Skinner, Steven A, Kaufmann, Walter E, Miller, Jennifer L, Driscoll, Daniel J, Bird, Lynne M, Butler, Merlin G, Dykens, Elisabeth M, Gold, June-Anne, Kimonis, Virginia, Bacino, Carlos A, Tan, Wen-Hann, Kothare, Sanjeev V, Peters, Sarika U, Percy, Alan K, Glaze, Daniel G

مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Neurosciences, Lung, Pediatric, Rare Diseases, Behavioral and Social Science, Intellectual and Developmental Disabilities (IDD), Genetics, Mental Health, Clinical Research, Sleep Research, Neurodegenerative, Brain Disorders, Adolescent, Angelman Syndrome, Child, Child, Preschool, Humans, Neurodevelopmental Disorders, Prader-Willi Syndrome, Rett Syndrome, Sleep Wake Disorders, Pediatric sleep, Rare disease, Genetic syndromes, Neurodevelopment, Paediatrics and Reproductive Medicine, Neurology & Neurosurgery, Paediatrics

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6zx0t3drTest

المؤلفون: O'Neill, Gordon C., MajDriscoll, Daniel A., Jr, Maj

المصدر: Marine Corps Gazette. 05/1991 75(5):76-83

مصطلحات موضوعية: MANEUVER WARFARE, MARINE CORPS AVIATION

الوصول الحر: http://www.dtic.mil/dtic/aulimp/citations/gsa/1991_112837/84378.htmlTest

المؤلفون: Mahmoud, Ranim, Leonenko, Anna, Butler, Merlin G, Flodman, Pamela, Gold, June‐Anne, Miller, Jennifer L, Roof, Elizabeth, Dykens, Elisabeth, Driscoll, Daniel J, Kimonis, Virginia

المصدر: Clinical Genetics. 100(1)

مصطلحات موضوعية: Congenital Structural Anomalies, Clinical Research, Pediatric, Adolescent, Adult, Body Height, Child, Child, Preschool, Female, Growth Hormone, Humans, Infant, Male, Middle Aged, Phenotype, Prader-Willi Syndrome, Young Adult, dysmorphology, genetic subtypes, genotype–, phenotype, growth, growth hormone treatment, Prader‐, Willi syndrome, Prader-Willi syndrome, genotype-phenotype, Genetics, Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/96s8x853Test

المؤلفون: Montes, Andrea S, Osann, Kathryn E, Gold, June Anne, Tamura, Roy N, Driscoll, Daniel J, Butler, Merlin G, Kimonis, Virginia E

المصدر: Genes. 11(11)

مصطلحات موضوعية: PWS genetic subtype–phenotype correlations, PWS molecular classes, Prader-Willi syndrome, growth hormone treatment, natural history, psychiatric behavioral phenotype, PWS genetic subtype–, phenotype correlations, Genetics

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7vn2v4k6Test

المؤلفون: Tamura, Roy, Gold, June-Anne, Patel, Nidhi, Surampalli, Abhilasha, Miller, Jennifer, Roof, Elizabeth, Dykens, Elisabeth, Butler, Merlin, Driscoll, Daniel, Kimonis, Virginia, Manazir, Javeria

المصدر: Genes. 10(11)

مصطلحات موضوعية: Prader–Willi syndrome, age diagnosis, deletion, obesity, uniparental disomy, Age Factors, Child, Child, Preschool, Chromosomes, Human, Pair 15, Comorbidity, Early Diagnosis, Female, Genomic Imprinting, Hormone Replacement Therapy, Human Growth Hormone, Humans, Infant, Male, Obesity, Prader-Willi Syndrome, Rare Diseases

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/04q496dnTest

المؤلفون: Kimonis, Virginia E, Tamura, Roy, Gold, June-Anne, Patel, Nidhi, Surampalli, Abhilasha, Manazir, Javeria, Miller, Jennifer L, Roof, Elizabeth, Dykens, Elisabeth, Butler, Merlin G, Driscoll, Daniel J

المصدر: Genes. 10(11)

مصطلحات موضوعية: Prader–Willi syndrome, age diagnosis, deletion, obesity, uniparental disomy, Prader-Willi syndrome, Brain Disorders, Prevention, Intellectual and Developmental Disabilities (IDD), Congenital Structural Anomalies, Nutrition, Obesity, Pediatric, Genetics, Clinical Research, Rare Diseases, 2.1 Biological and endogenous factors, Oral and Gastrointestinal, Metabolic and Endocrine, Intellectual and Developmental Disabilities

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/35w990kcTest

المؤلفون: Butler, Merlin G, Kimonis, Virginia, Dykens, Elisabeth, Gold, June Anne, Tamura, Roy, Miller, Jennifer L, Driscoll, Daniel J

المصدر: American Journal of Medical Genetics Part A. 179(8)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Pediatric, Good Health and Well Being, Adolescent, Adult, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 15, Cohort Studies, Female, Gametogenesis, Genetic Testing, Humans, Infant, Male, Occupational Exposure, Occupations, Prader-Willi Syndrome, Seasons, Sex Factors, United States, birth seasonality, environmental factors, Prader-Willi syndrome, PWS genetic subtypes, Clinical Sciences, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7mf391szTest

المؤلفون: Butler, Merlin G, Hartin, Samantha N, Hossain, Waheeda A, Manzardo, Ann M, Kimonis, Virginia, Dykens, Elisabeth, Gold, June Anne, Kim, Soo-Jeong, Weisensel, Nicolette, Tamura, Roy, Miller, Jennifer L, Driscoll, Daniel J

المصدر: Journal of Medical Genetics. 56(3)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Pediatric, Obesity, Clinical Research, Adolescent, Adult, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 15, Cohort Studies, DNA Copy Number Variations, Female, Genetic Association Studies, Genetic Markers, Genetic Predisposition to Disease, Genetic Testing, Humans, Infant, Male, Middle Aged, Mutation, Polymorphism, Single Nucleotide, Prader-Willi Syndrome, Young Adult, PWS maternal disomy subclasses, Prader-Willi syndrome, maternal age effects, molecular genetic classification, pws deletion subtypes, Medical and Health Sciences, Genetics & Heredity, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5kh5z9z3Test

المؤلفون: Kweh, Frederick A., Sulsona, Carlos R., Miller, Jennifer L., Driscoll, Daniel J.

المساهمون: National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Defense

المصدر: Obesity Science & Practice ; volume 9, issue 4, page 383-394 ; ISSN 2055-2238 2055-2238

الإتاحة: https://doi.org/10.1002/osp4.663Test