المؤلفون: Smeland, Olav B, Shadrin, Alexey, Bahrami, Shahram, Broce, Iris, Tesli, Martin, Frei, Oleksandr, Wirgenes, Katrine V, O'Connell, Kevin S, Krull, Florian, Bettella, Francesco, Steen, Nils Eiel, Sugrue, Leo, Wang, Yunpeng, Svenningsson, Per, Sharma, Manu, Pihlstrøm, Lasse, Toft, Mathias, O'Donovan, Michael, Djurovic, Srdjan, Desikan, Rahul, Dale, Anders M, Andreassen, Ole A

المصدر: Biological Psychiatry. 89(3)

مصطلحات موضوعية: Genetics, Biotechnology, Aging, Parkinson's Disease, Neurodegenerative, Serious Mental Illness, Human Genome, Neurosciences, Prevention, Mental Health, Schizophrenia, Brain Disorders, 2.1 Biological and endogenous factors, Aetiology, Neurological, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Multifactorial Inheritance, Parkinson Disease, Polymorphism, Single Nucleotide, GWAS, Genetic overlap, Parkinson’s disease, RERE, ZDHHC2, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9m0551bc

المؤلفون: Jordan, Valerie K, Fregeau, Brieana, Ge, Xiaoyan, Giordano, Jessica, Wapner, Ronald J, Balci, Tugce B, Carter, Melissa T, Bernat, John A, Moccia, Amanda N, Srivastava, Anshika, Martin, Donna M, Bielas, Stephanie L, Pappas, John, Svoboda, Melissa D, Rio, Marlène, Boddaert, Nathalie, Cantagrel, Vincent, Lewis, Andrea M, Scaglia, Fernando, Network, Undiagnosed Diseases, Kohler, Jennefer N, Bernstein, Jonathan A, Dries, Annika M, Rosenfeld, Jill A, DeFilippo, Colette, Thorson, Willa, Yang, Yaping, Sherr, Elliott H, Bi, Weimin, Scott, Daryl A

المصدر: Human Mutation. 39(5)

مصطلحات موضوعية: Congenital Structural Anomalies, Genetics, Genetic Testing, Rare Diseases, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Carrier Proteins, Child, Preschool, Fatal Outcome, Female, Genetic Association Studies, Humans, Infant, Male, Mutation, Young Adult, 1p36 deletion syndrome, CHARGE syndrome, CHD7, genotype-phenotype correlations, NEDBEH, RERE, Undiagnosed Diseases Network, Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/57z6f57h

المؤلفون: Chai, Yuan, author, Kunda, Titus Kubri Kajo, author, Rodríguez, Alejandro, author, Rose, Sharon, author

المصدر: Prosody and Prosodic Interfaces, 2022, ill.

الإتاحة: https://doi.org/10.1093/oso/9780198869740.003.0011

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المؤلفون: Strawbridge, Renée Thérèse, Mills, Amanda

المصدر: New Zealand musician (Online), 23 Dec 2022
NZ musician

URL الوصول: https://nzmusician.co.nz/music/goldsmith-baynes-e-rere-ra-2/
https://ndhadeliver.natlib.govt.nz/webarchive/20230112203525mp_/https://nzmusician.co.nz/music/goldsmith-baynes-e-rere-ra-2/
https://nzmusician.co.nz/music/sjd-sweetheart-2/
https://ndhadeliver.natlib.govt.nz/webarchive/20230112203525mp_/https://nzmusician.co.nz/music/sjd-sweetheart-2/

المساهمون: Flowers, L

المصدر: Conference: Windpower '98, Bakersfield, CA (US), 04/27/1998--05/01/1998; Other Information: Supercedes report DE98003980; PBD: Jul 1998; PBD: 1 Jul 1998

وصف الملف: Medium: ED; Size: 6 pages

URL الوصول: http://www.osti.gov/scitech/servlets/purl/629403

المؤلفون: Bum Jun Kim, Hitisha P. Zaveri, Valerie K. Jordan, Andres Hernandez-Garcia, Daron J. Jacob, Diana L. Zamora, Wei Yu, Robert J. Schwartz, Daryl A. Scott

المصدر: Disease Models & Mechanisms, Vol 11, Iss 9 (2018)

مصطلحات موضوعية: RERE, GATA4, Atrioventricular canal, Atrioventricular cushion, Endothelial-to-mesenchymal transition, Ventricular septal defects, Medicine, Pathology, RB1-214

وصف الملف: electronic resource

Relation: http://dmm.biologists.org/content/11/9/dmm031534; https://doaj.org/toc/1754-8403; https://doaj.org/toc/1754-8411

URL الوصول: https://doaj.org/article/a9ce8e98bdaa403b92be87c363a87bf4

المؤلفون: Tūranga Health

المصدر: Pīpīwharauroa (Gisborne, N.Z.), Hōn 2019; v.26 n.7:p.15

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المؤلفون: Wylie, Liz

المصدر: Wanganui chronicle, 23 Jun 2018; sup.p.4