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1دورية أكاديمية
المؤلفون: Slavotinek, Anne, Kaylor, Julie, Pierce, Heather, Cahr, Michelle, DeWard, Stephanie J, Schneidman-Duhovny, Dina, Alsadah, Adnan, Salem, Fadi, Schmajuk, Gabriela, Mehta, Lakshmi
المصدر: American Journal of Human Genetics. 96(1)
مصطلحات موضوعية: Reproductive Medicine, Biomedical and Clinical Sciences, Kidney Disease, Clinical Research, Genetics, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Renal and urogenital, Amniotic Fluid, Carrier Proteins, Child, Female, Fetus, Genetic Variation, Humans, Hydrocephalus, Male, Membrane Proteins, Nephrotic Syndrome, Phenotype, Pregnancy, Protein Structure, Secondary, alpha-Fetoproteins, Biological Sciences, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/7943r1m9Test
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2دورية أكاديمية
المؤلفون: Vulto-van Silfhout, Anneke T, Nakagawa, Tadashi, Bahi-Buisson, Nadia, Haas, Stefan A, Hu, Hao, Bienek, Melanie, Vissers, Lisenka ELM, Gilissen, Christian, Tzschach, Andreas, Busche, Andreas, Müsebeck, Jörg, Rump, Patrick, Mathijssen, Inge B, Avela, Kristiina, Somer, Mirja, Doagu, Fatma, Philips, Anju K, Rauch, Anita, Baumer, Alessandra, Voesenek, Krysta, Poirier, Karine, Vigneron, Jacqueline, Amram, Daniel, Odent, Sylvie, Nawara, Magdalena, Obersztyn, Ewa, Lenart, Jacek, Charzewska, Agnieszka, Lebrun, Nicolas, Fischer, Ute, Nillesen, Willy M, Yntema, Helger G, Järvelä, Irma, Ropers, Hans-Hilger, de Vries, Bert BA, Brunner, Han G, van Bokhoven, Hans, Raymond, F Lucy, Willemsen, Michèl AAP, Chelly, Jamel, Xiong, Yue, Barkovich, A James, Kalscheuer, Vera M, Kleefstra, Tjitske, de Brouwer, Arjan PM
المصدر: Human Mutation. 36(1)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Clinical Research, Intellectual and Developmental Disabilities (IDD), Brain Disorders, Neurosciences, Pediatric, Rare Diseases, Congenital Structural Anomalies, Aetiology, 2.1 Biological and endogenous factors, Neurological, Adolescent, Adult, Brain, Cell Cycle Proteins, Cells, Cultured, Child, Child, Preschool, Cullin Proteins, Genetic Association Studies, HEK293 Cells, Humans, Infant, Male, Malformations of Cortical Development, Mental Retardation, X-Linked, Middle Aged, Nerve Tissue Proteins, Pedigree, Sequence Analysis, DNA, Young Adult, CUL4B, WDR62, cortical dysplasia, hydrocephalus, intellectual disability, mutation, Clinical Sciences, Genetics & Heredity, Clinical sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/7h5466vkTest
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3دورية أكاديمية
المؤلفون: Yoon, Michael K, Parsa, Andrew T, Horton, Jonathan C
المصدر: Journal of Neurosurgery Pediatrics. 11(6)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Ophthalmology and Optometry, Physical Injury - Accidents and Adverse Effects, Neurosciences, Brain Disorders, Traumatic Head and Spine Injury, Dental/Oral and Craniofacial Disease, Rare Diseases, 2.1 Biological and endogenous factors, Aetiology, Adult, Brain Injuries, Child, Chronic Disease, Disease Progression, Enophthalmos, Equipment Design, Humans, Intracranial Hypotension, Magnetic Resonance Imaging, Male, Paranasal Sinuses, Pneumocephalus, Sella Turcica, Skull, Tomography, X-Ray Computed, Ventriculoperitoneal Shunt, enophthalmos, ventriculoperitoneal shunt, cerebrospinal fluid, hydrocephalus, pneumocephalus, Sunken Eyes, Sagging Brain Syndrome, Paediatrics and Reproductive Medicine, Neurology & Neurosurgery, Paediatrics
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/8633d0m9Test