المؤلفون: Campbell, Linda E.^{Aff1, IDs41252023003867_cor1}, Corliss, Clare, Green, Nicola, Duijff, Sasja, Roche, Laura

المصدر: Advances in Neurodevelopmental Disorders: Multidisciplinary Research and Practice Across the Lifespan. :1-13

المؤلفون: Swan, Tricia B.^Aff3, Martinez, Carmen J.^Aff4

المساهمون: Zeretzke-Bien, Cristina M., editor^Aff1, Swan, Tricia B., editor^Aff2

المصدر: Quick Hits for Pediatric Emergency Medicine. :115-125

المؤلفون: Ana Paula Corrêa Cabral, Dafne Dain Gandelman Horovitz, Lidiane Nogueira Santos, Amanda Oliveira de Carvalho, Cristina Maria Duarte Wigg, Luciana Castaneda, Liane Simon, Carla Trevisan Martins Ribeiro

المصدر: Children, Vol 11, Iss 7, p 767 (2024)

مصطلحات موضوعية: 22q11.2 deletion syndrome, velo-cardio-facial syndrome, International Classification of Functioning, Disability and Health, child, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2227-9067/11/7/767; https://doaj.org/toc/2227-9067

URL الوصول: https://doaj.org/article/028cb89ea76f40979290cead62ecbc96

المؤلفون: Ana A. Francisco, John J. Foxe, Sophie Molholm

المصدر: Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-15 (2023)

مصطلحات موضوعية: EEG, Velo-cardio-facial syndrome, DiGeorge syndrome, Schizophrenia, Sensory processing, Response inhibition, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1866-1955

URL الوصول: https://doaj.org/article/1782c17d7cbc451ebf94f8ee07e83c39

المؤلفون: Campbell, L. E.^{Aff1, Aff2, IDs10803021051729_cor1}, Swaab, L., Freeman, E. E.^{Aff1, Aff6}, McCormack, L., Simon, T. J.^{Aff3, Aff4}, Angkustsiri, K.^{Aff4, Aff5}, McCabe, K. L.^{Aff3, Aff4}

المصدر: Journal of Autism and Developmental Disorders. 52(7):3076-3087

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المؤلفون: Van Den Heuvel, Ellen^{Aff2, Aff3}, Breckpot, Jeroen^{Aff2, Aff3}, Vergaelen, Elfi^{Aff2, Aff3}, Swillen, Ann^{Aff2, Aff3}

المساهمون: Cummings, Louise, editor^Aff1

المصدر: Handbook of Pragmatic Language Disorders : Complex and Underserved Populations. :163-194

المؤلفون: Guo, Tingwei, Repetto, Gabriela M, McDonald McGinn, Donna M, Chung, Jonathan H, Nomaru, Hiroko, Campbell, Christopher L, Blonska, Anna, Bassett, Anne S, Chow, Eva WC, Mlynarski, Elisabeth E, Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E, Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E, Digilio, M Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E, Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E, Tassone, Flora, Simon, Tony J, van Duin, Esther DA, van Amelsvoort, Thérèse A, Kates, Wendy R, Zackai, Elaine, Johnston, H Richard, Cutler, David J, Agopian, AJ, Goldmuntz, Elizabeth, Mitchell, Laura E, Wang, Tao, Emanuel, Beverly S, Morrow, Bernice E

المصدر: Circulation Genomic and Precision Medicine. 10(5)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Genetics, Rare Diseases, Congenital Structural Anomalies, Clinical Research, Human Genome, Heart Disease, Cardiovascular, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Congenital, Chromatin, Chromosomes, Human, Pair 5, DiGeorge Syndrome, Genetic Loci, Genome-Wide Association Study, Genotype, High-Throughput Nucleotide Sequencing, Humans, Linkage Disequilibrium, MEF2 Transcription Factors, Oligonucleotide Array Sequence Analysis, Phenotype, Polymorphism, Single Nucleotide, Receptors, G-Protein-Coupled, Sequence Analysis, DNA, Tetralogy of Fallot, chromosomes, DiGeorge syndrome, genotype, ivelo-cardio-facial syndrome, tetralogy of Fallot, International 22q11.2 Consortium/Brain and Behavior Consortium*, Medical Biotechnology, Cardiorespiratory Medicine and Haematology, Cardiovascular System & Hematology, Cardiovascular medicine and haematology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7hp1507k

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