Vyzkoušejte nový nástroj s podporou AI
  
        
        Summon Research Assistant
        BETA
      
                    
  
      
    Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
                                      
                                            Shinawi, Marwan,                              Liu, Pengfei,                              Kang, Sung-Hae L,                              Shen, Joseph,                              Belmont, John W,                              Scott, Daryl A,                              Probst, Frank J,                              Craigen, William J,                              Graham, Brett H,                              Pursley, Amber,                              Clark, Gary,                              Lee, Jennifer,                              Proud, Monica,                              Stocco, Amber,                              Rodriguez, Diana L,                              Kozel, Beth A,                              Sparagana, Steven,                              Roeder, Elizabeth R,                              McGrew, Susan G,                              Kurczynski, Thaddeus W,                              Allison, Leslie J,                              Amato, Stephen,                              Savage, Sarah,                              Patel, Ankita,                              Stankiewicz, Pawel,                              Beaudet, Arthur L,                              Cheung, Sau Wai,                              Lupski, James R                              
Published in Journal of medical genetics (01.05.2010)
                   
      
      
                                                  Published in Journal of medical genetics (01.05.2010)
Get full text
              Journal Article
          
              
          Abnormal Brain Connectivity Patterns in Children with Global Developmental Delay Accompanied by Cognitive Impairment: A Resting-State EEG Study
                                      
                                            Hui, Zhichong,                              Zhang, Yi,                              Su, Yuwei,                              Kang, Jiaming,                              Qi, Weihang,                              Li, Shaoqing,                              Zhang, Jiamei,                              Shi, Kaili,                              Wang, Mingmei,                              Yang, Yonghui,                              Zhang, Guangyu,                              Yang, Lei,                              Chen, Gongxun,                              Li, Sansong,                              Hu, Yuxia,                              Zhu, Dengna                              
Published in Journal of integrative neuroscience (30.09.2025)
                   
      
      
                                                  Published in Journal of integrative neuroscience (30.09.2025)
Get full text
              Journal Article
          
              
          Whole Exome Sequencing and Panel-Based Analysis in 176 Spanish Children with Neurodevelopmental Disorders: Focus on Autism Spectrum Disorder and/or Intellectual Disability/Global Developmental Delay
                                      
                                            Sánchez Suárez, Ariadna,                              Martínez Menéndez, Beatriz,                              Escolar Escamilla, Eduardo,                              Martínez Sarries, Francisco J.,                              Esparza Garrido, Miren Iranzu,                              Gil-Fournier, Belén,                              Ramiro León, Soraya,                              Rubio Gribble, Bárbara,                              Quesada Espinosa, Juan F.,                              Alcaraz Romero, Andrés J.                              
Published in Genes (11.10.2024)
                   
      
      
                                                  Published in Genes (11.10.2024)
Get full text
              Journal Article
          
              
          Iron deficiency in children with global developmental delay and autism spectrum disorder
                                      
                                            Sidrak, Samuel,                              Yoong, Terence,                              Woolfenden, Susan                              
Published in Journal of paediatrics and child health (01.05.2014)
                   
      
      
                                                  Published in Journal of paediatrics and child health (01.05.2014)
Get full text
              Journal Article
          
              
          Role of Corpus Callosum in Global Developmental Delay
                                      
                                            K Mounisha,                              MU Jeevika,                              BG Mahesh,                              B Adarsh,                              KK Nirnay                              
Published in Asian Journal of Medical Radiological Research (05.07.2020)
                   
      
      
                                                  Published in Asian Journal of Medical Radiological Research (05.07.2020)
Get full text
              Journal Article
          
              
          Diagnostic Yield of Intellectual Disability Gene Panels
                                      
                                            Pekeles, Heather,                              Accogli, Andrea,                              Boudrahem-Addour, Nassima,                              Russell, Laura,                              Parente, Fabienne,                              Srour, Myriam                              
Published in Pediatric neurology (01.03.2019)
                   
      
      
                                                  Published in Pediatric neurology (01.03.2019)
Get full text
              Journal Article
          
              
          Adaptive behaviour deficits in individuals with 3q29 deletion syndrome
                                      
                                            Pollak, R. M.,                              Burrell, T. L.,                              Cubells, J. F.,                              Klaiman, C.,                              Murphy, M. M.,                              Saulnier, C. A.,                              Walker, E. F.,                              White, S. P.,                              Mulle, J. G.                              
Published in Journal of intellectual disability research (01.02.2024)
                   
      
      
                                                  Published in Journal of intellectual disability research (01.02.2024)
Get full text
              Journal Article
          
              
          Changes in social functioning and engagement during canine-assisted intervention for children with neurodevelopmental disorders in the context of an early intervention service
                                      
                                            Ávila-Álvarez, Adriana,                              Alonso-Bidegain, Miguel,                              Ramos-Veiguela, Daniel,                              Iglesias-Jove, Elba,                              De-Rosende-Celeiro, Iván                              
Published in Research in developmental disabilities (01.05.2022)
                   
      
      
                                                  Published in Research in developmental disabilities (01.05.2022)
Get full text
              Journal Article
          
              
          Guideline recommendations for diagnosis and clinical management of Ring14 syndrome—first report of an ad hoc task force
                                      
                                            Rinaldi, Berardo,                              Vaisfeld, Alessandro,                              Amarri, Sergio,                              Baldo, Chiara,                              Gobbi, Giuseppe,                              Magini, Pamela,                              Melli, Erto,                              Neri, Giovanni,                              Novara, Francesca,                              Pippucci, Tommaso,                              Rizzi, Romana,                              Soresina, Annarosa,                              Zampini, Laura,                              Zuffardi, Orsetta,                              Crimi, Marco                              
Published in Orphanet journal of rare diseases (11.04.2017)
                   
      
      
                                                  Published in Orphanet journal of rare diseases (11.04.2017)
Get full text
              Journal Article