Search Results - "intellectually disabled"

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  1. 1061
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    Novel loss-of-function variants in WDR26 cause Skraban-Deardorff syndrome in two Chinese patients by Qi Yang, Qi Yang, Xunzhao Zhou, Xunzhao Zhou, Sheng Yi, Sheng Yi, XiaoLing Li, Qiang Zhang, Qiang Zhang, Shujie Zhang, Shujie Zhang, Li Lin, Li Lin, Shang Yi, Shang Yi, Biyan Chen, Biyan Chen, Zailong Qin, Zailong Qin, Jingsi Luo, Jingsi Luo, Jingsi Luo

    Published 2024
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  2. 1062
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    PROGRAM PENGEMBANGAN KETERAMPILAN VOKASIONAL BERBASIS POTENSI DAERAH BAGI ANAK DENGAN HAMBATAN KECERDASAN RINGAN DI SLB AL - HASYEMI by Pepi Nurinsi Alawiyah, -

    Published 2021
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  3. 1063
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    Latest Findings in Intellectual and Developmental Disabilities Research

    Published 2012
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  4. 1064
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    Developmental Disabilities Molecules Involved, Diagnosis, and Clinical Care

    Published 2013
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  5. 1065
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    An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndrome by Eleonora Maino, Ori Scott, Samar Z. Rizvi, Wing Suen Chan, Shagana Visuvanathan, Youssif Ben Zablah, Hongbin Li, Ameet S. Sengar, Michael W. Salter, Zhengping Jia, Janet Rossant, Ronald D. Cohn, Bin Gu, Evgueni A. Ivakine

    Published 2024
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  6. 1066
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    Fatty Acyl-CoA Reductase 1 Deficiency by Charles N Swisher

    Published 2015
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  7. 1067
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    When Feeding Difficulties Are due to Genetics by Laura Travan, Maria Santa Rocca, Francesca Buonomo, Lisa Cleva, Vanna Pecile, Angela De Cunto

    Published 2015
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  8. 1068
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    Une étude du rapport au savoir d'enfants scolarisés en IME dans le cadre d'un parcours artistique by Céline Salles, Florence Savournin

    Published 2015
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  9. 1069
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    Cardiorespiratory Fitness

    Published 2020
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  10. 1070
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    NR2F1 shapes mitochondria in the mouse brain, providing new insights into Bosch-Boonstra-Schaaf optic atrophy syndrome by Sara Bonzano, Eleonora Dallorto, Ivan Molineris, Filippo Michelon, Isabella Crisci, Giovanna Gambarotta, Francesco Neri, Salvatore Oliviero, Ruth Beckervordersandforth, Dieter Chichung Lie, Paolo Peretto, Serena Bovetti, Michèle Studer, Silvia De Marchis

    Published 2023
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  11. 1071
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    Inherited Developmental and Epileptic Encephalopathies by Emanuele Bartolini

    Published 2021
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  12. 1072
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    My home - the hospital: A case study by D.D. Jaftha

    Published 1984
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  13. 1073
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    Taf1 knockout is lethal in embryonic male mice and heterozygous females show weight and movement disorders by Elisa M. Crombie, Andrea J. Korecki, Karen Cleverley, Bethany A. Adair, Thomas J. Cunningham, Weaverly Colleen Lee, Tess C. Lengyell, Cheryl Maduro, Victor Mo, Liam M. Slade, Ines Zouhair, Elizabeth M. C. Fisher, Elizabeth M. Simpson

    Published 2024
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  14. 1074
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    The Value of Imagistics in Early Diagnosis of Tuberous Sclerosis by Claudia Ioana Borțea, Vlad Laurentiu David, Florina Stoica, Cezara Mureșan, Marioara Boia

    Published 2020
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  15. 1075
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    Ovarian torsion secondary to serous cystadenoma in a patient with MOMO syndrome by Jay Patel, Kriti Tiwari, Anthony Tsai

    Published 2021
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  16. 1076
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    Autonomy Benefits and Risks of Assistive Technologies for Persons With Intellectual and Developmental Disabilities by Fiachra O'Brolcháin

    Published 2018
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  17. 1077
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    Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated pheno... by Darina Prchalova, Marketa Havlovicova, Katalin Sterbova, Viktor Stranecky, Miroslava Hancarova, Zdenek Sedlacek

    Published 2017
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  18. 1078
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    CNNM2-Related Disorders: Phenotype and Its Severity Were Associated With the Mode of Inheritance by Han Zhang, Ye Wu, Yuwu Jiang

    Published 2021
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  19. 1079
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    A partial <it>MECP2</it> duplication in a mildly affected adult male: a putative role for the 3' untranslated region in the <it>MECP2</it> duplication phenotype by Hanchard Neil A, Carvalho Claudia MB, Bader Patricia, Thome Aaron, Omo-Griffith Lisa, del Gaudio Daniela, Pehlivan Davut, Fang Ping, Schaaf Christian P, Ramocki Melissa B, Lupski James R, Cheung Sau Wai

    Published 2012
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  20. 1080
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    Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in China by Miriam Kessi, Baiyu Chen, Li-Dan Shan, Ying Wang, Lifen Yang, Fei Yin, Fang He, Jing Peng, Guoli Wang

    Published 2023
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