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1دورية أكاديمية
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
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2دورية أكاديمية
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
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3دورية أكاديمية
المؤلفون: Oldzej, Jeannine, Manazir, Javeria, Gold, June‐Anne, Mahmoud, Ranim, Osann, Kathryn, Flodman, Pamela, Cassidy, Suzanne B, Kimonis, Virginia E
المصدر: American Journal of Medical Genetics Part A. 182(1)
مصطلحات موضوعية: Paediatrics, Biomedical and Clinical Sciences, Congenital Structural Anomalies, Pediatric, Rare Diseases, Clinical Research, Adolescent, Body Height, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 15, Cytogenetic Analysis, Exotropia, Female, Genomic Imprinting, Growth Hormone, Humans, Male, Phenotype, Prader-Willi Syndrome, Uniparental Disomy, dysmorphology, GH, imprinting disorders, microdeletion, Prader-Willi syndrome, uniparental disomy, Genetics, Clinical Sciences, Clinical sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/6n74k0nwTest
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4دورية أكاديمية
المؤلفون: Qian, Emily, Thong, Meow-Keong, Flodman, Pamela, Gargus, Jay
المصدر: Journal of Community Genetics. 10(3)
مصطلحات موضوعية: Biological Sciences, Genetics, Health Services, Clinical Research, Generic health relevance, Good Health and Well Being, Genetic counseling, Genetics services, Malaysia, Provider knowledge, Rare disease, Southeast Asia
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/5hf9f992Test
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5دورية أكاديمية
المؤلفون: Smith, Moyra, Flodman, Pamela L
مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Human Genome, Biotechnology, Generic health relevance, enhancers, transcription, domains, modifications malformations, enhancer, epigenetic, malformation, structural damage, Biochemistry and cell biology, Medical biochemistry and metabolomics
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/2nc7p31nTest
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6دورية أكاديمية
المؤلفون: Ranim Mahmoud, Heidi D. Swanson, Merlin G. Butler, Pamela Flodman, June-Anne Gold, Jennifer L. Miller, Elizabeth Roof, Kathryn Osann, Elisabeth Dykens, Daniel J. Driscoll, Virginia Kimonis
المصدر: Journal of Clinical Medicine, Vol 11, Iss 9, p 2572 (2022)
مصطلحات موضوعية: Prader–Willi syndrome, behavior, genetic subtypes, growth hormone, Medicine
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Greenwood, Jaclyn, Flodman, Pamela, Osann, Kathryn, Boyadjiev, Simeon A, Kimonis, Virginia
المصدر: Genetics in Medicine. 16(4)
مصطلحات موضوعية: Biological Sciences, Genetics, Rare Diseases, Congenital Structural Anomalies, Pediatric, Dental/Oral and Craniofacial Disease, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Child, Child, Preschool, Cranial Sutures, Craniosynostoses, Female, Health Surveys, Humans, Incidence, Infant, Male, Pedigree, Phenotype, Risk Factors, Young Adult, familial incidence, nonsyndromic craniosynostosis, symptoms, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/1mb7051qTest
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8دورية أكاديمية
المؤلفون: Gold, June-Anne, Ruth, Chelsey, Osann, Kathryn, Flodman, Pamela, McManus, Barbara, Lee, Hye-Seung, Donkervoort, Sandra, Khare, Manaswitha, Roof, Elizabeth, Dykens, Elizabeth, Miller, Jennifer, Driscoll, Daniel, Butler, Merlin, Heinemann, Janalee, Cassidy, Suzanne, Kimonis, Virginia
المصدر: Genetics in Medicine. 16(2)
مصطلحات موضوعية: Chromosomes, Human, Pair 15, Genomic Imprinting, Health Surveys, Humans, Prader-Willi Syndrome, Reproductive Techniques, Assisted, Twins, Uniparental Disomy
وصف الملف: application/pdf
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9دورية أكاديمية
المؤلفون: Gold, JA, Ruth, C, Osann, K, Flodman, P, McManus, B, Lee, HS, Donkervoort, S, Khare, M, Roof, E, Dykens, E, Milller, JL, Driscoll, DJ, Butler, MG, Heinemann, J, Cassidy, S, Kimonis, VE
المصدر: Genetics in Medicine. 15(11)
مصطلحات موضوعية: Genetics, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/4813h4z7Test
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10دورية أكاديمية
المؤلفون: Kiersten Flodman, Ivan R. Corrêa, Nan Dai, Peter Weigele, Shuang-yong Xu
المصدر: Frontiers in Microbiology, Vol 11 (2020)
مصطلحات موضوعية: Type II restriction, modified phage genome, phage SP8, phage Xp12 genome sequence, 5hmdU DNA kinase, Microbiology, QR1-502
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fmicb.2020.604618/fullTest; https://doaj.org/toc/1664-302XTest