المؤلفون: Gilliand, M., Perrenoud, B., Lecerf, T., Serex, M., Breaud, A., Larkin, P.

المصدر: JBI evidence synthesis, vol. 21, no. 1, pp. 254-263

مصطلحات موضوعية: Adult, Humans, Intellectual Disability/complications, Intellectual Disability/diagnosis, Pain/diagnosis, Pain Measurement, Review Literature as Topic, Systematic Reviews as Topic

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36000781; info:eu-repo/semantics/altIdentifier/eissn/2689-8381; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_EFAB6C345AB63; https://serval.unil.ch/notice/serval:BIB_EFAB6C345AB6Test; urn:issn:2689-8381; https://serval.unil.ch/resource/serval:BIB_EFAB6C345AB6.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_EFAB6C345AB63Test

الإتاحة: https://doi.org/10.11124/JBIES-21-00434Test
https://serval.unil.ch/notice/serval:BIB_EFAB6C345AB6Test
https://serval.unil.ch/resource/serval:BIB_EFAB6C345AB6.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_EFAB6C345AB63Test

المؤلفون: Peluso, Francesca, Caraffi, Stefano G., Contro& amp, grave, Gianluca, Valeri, Lara, Napoli, Manuela, Carboni, Giorgia, Seth, Alka, Zuntini, Roberta, Coccia, Emanuele, Astrea, Guja, Bisgaard, Anne Marie, Ivanovski, Ivan, Maitz, Silvia, Brischoux-Boucher, Elise, Carter, Melissa T., Dentici, Maria Lisa, Devriendt, Koenraad, Bellini, Melissa, Digilio, Maria Cristina, Doja, Asif, Dyment, David A., Farholt, Stense, Ferreira, Carlos R., Wolfe, Lynne A., Gahl, William A., Gnazzo, Maria, Goel, Himanshu, Grønborg, Sabine Weller, Hammer, Trine, Iughetti, Lorenzo, Kleefstra, Tjitske, Koolen, David A., Lepri, Francesca Romana, Lemire, Gabrielle, Louro, Pedro, McCullagh, Gary, Madeo, Simona F., Milone, Annarita, Milone, Roberta, Nielsen, Jens Erik Klint, Novelli, Antonio, Ockeloen, Charlotte W., Pascarella, Rosario, Pippucci, Tommaso, Ricca, Ivana, Robertson, Stephen P., Sawyer, Sarah, Falkenberg Smeland, Marie, Stegmann, Sander, Stumpel, Constanze T., Goel, Amy, Taylor, Juliet M., Barbuti, Domenico, Soresina, Annarosa, Bedeschi, Maria Francesca, Battini, Roberta, Cavalli, Anna, Fusco, Carlo, Iascone, Maria, Van Maldergem, Lionel, Venkateswaran, Sunita, Zuffardi, Orsetta, Vergano, Samantha, Garavelli, Livia, Bayat, Allan

المصدر: Peluso , F , Caraffi , S G , Contro& amp; grave; , G , Valeri , L , Napoli , M , Carboni , G , Seth , A , Zuntini , R , Coccia , E , Astrea , G , Bisgaard , A M , Ivanovski , I , Maitz , S , Brischoux-Boucher , E , Carter , M T , Dentici , M L , Devriendt , K , Bellini , M , Digilio , M C , Doja , A , Dyment , D A , Farholt , S , Ferreira , C ....

مصطلحات موضوعية: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Research, Pathological Conditions, Signs and Symptoms, Patient Care, Radiology, Neuroimaging, Tooth Abnormalities/diagnostic imaging, Bone Diseases, Developmental/diagnostic imaging, Humans, Repressor Proteins/genetics, Phenotype, Facies, Intellectual Disability/diagnosis, Transcription Factors, Abnormalities, Multiple/diagnosis

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/7d3c089e-d59c-49d7-aea3-705f49a98644Test

الإتاحة: https://doi.org/10.1136/jmg-2023-109141Test
https://portal.findresearcher.sdu.dk/da/publications/7d3c089e-d59c-49d7-aea3-705f49a98644Test
https://findresearcher.sdu.dk/ws/files/251163717/Open_Access_Version.pdfTest

المؤلفون: Lanvin, Pierre-Louis, Goronflot, Thomas, Isidor, Bertrand, Nizon, Mathilde, Durand, Benjamin, El Chehadeh, Salima, Geneviève, David, Ruault, Valentin, Fradin, Mélanie, Pasquier, Laurent, Thévenon, Julien, Delobel, Bruno, Burglen, Lydie, Afenjar, Alexandra, Faivre, Laurence, Francannet, Christine, Guerrot, Anne-Marie, Goldenberg, Alice, Mercier, Sandra, Héron, Delphine, Lehalle, Daphné, Mignot, Cyril, Marey, Isabelle, Charles, Perrine, Moutton, Sébastien, Bézieau, Stéphane, Bayat, Allan, Piton, Amélie, Willems, Marjolaine, Vincent, Marie

المصدر: Lanvin , P-L , Goronflot , T , Isidor , B , Nizon , M , Durand , B , El Chehadeh , S , Geneviève , D , Ruault , V , Fradin , M , Pasquier , L , Thévenon , J , Delobel , B , Burglen , L , Afenjar , A , Faivre , L , Francannet , C , Guerrot , A-M , Goldenberg , A , Mercier , S , Héron , D , Lehalle , D , Mignot , C , Marey , I , Charles , P , Moutton , ....

مصطلحات موضوعية: Male, Female, Child, Humans, Microcephaly/diagnosis, Growth Charts, Intellectual Disability/diagnosis, Syndrome, Body Mass Index, Body Height/genetics

الإتاحة: https://doi.org/10.1002/ajmg.a.63412Test
https://curis.ku.dk/portal/da/publications/growth-charts-in-dyrk1a-syndromeTest(b4e69c10-8cd0-4be2-b3d3-83fb10d21cf8).html

المؤلفون: Loberti, L., Bruno, L.P., Granata, S., Doddato, G., Resciniti, S., Fava, F., Carullo, M., Rahikkala, E., Jouret, G., Menke, L.A., Lederer, D., Vrielynck, P., Ryba, L., Brunetti-Pierri, N., Lasa-Aranzasti, A., Cueto-González, A.M., Trujillano, L., Valenzuela, I., Tizzano, E.F., Spinelli, A.M., Bruno, I., Currò, A., Stanzial, F., Benedicenti, F., Lopergolo, D., Santorelli, F.M., Aristidou, C., Tanteles, G.A., Maystadt, I., Tkemaladze, T., Reimand, T., Lokke, H., Õunap, K., Haanpää, M.K., Holubová, A., Zoubková, V., Schwarz, M., Žordania, R., Muru, K., Roht, L., Tihveräinen, A., Teek, R., Thomson, U., Atallah, I., Superti-Furga, A., Buoni, S., Canitano, R., Scandurra, V., Rossetti, A., Grosso, S., Battini, R., Baldassarri, M., Mencarelli, M.A., Rizzo, C.L., Bruttini, M., Mari, F., Ariani, F., Renieri, A., Pinto, A.M.

المصدر: Human molecular genetics, vol. 31, no. 24, pp. 4131-4142

مصطلحات موضوعية: Pregnancy, Female, Humans, Facies, Tooth Abnormalities/genetics, Bone Diseases, Developmental/genetics, Abnormalities, Multiple/genetics, Multiple/diagnosis, Intellectual Disability/genetics, Intellectual Disability/diagnosis, Comparative Genomic Hybridization, Repressor Proteins/genetics, Phenotype, Dwarfism/genetics, European People

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35861666; info:eu-repo/semantics/altIdentifier/eissn/1460-2083; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_CD40BBEC41D30; https://serval.unil.ch/notice/serval:BIB_CD40BBEC41D3Test; urn:issn:0964-6906; https://serval.unil.ch/resource/serval:BIB_CD40BBEC41D3.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_CD40BBEC41D30Test

الإتاحة: https://doi.org/10.1093/hmg/ddac167Test
https://serval.unil.ch/notice/serval:BIB_CD40BBEC41D3Test
https://serval.unil.ch/resource/serval:BIB_CD40BBEC41D3.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_CD40BBEC41D30Test

المؤلفون: Ruaud, Lyse, Drunat, Séverine, Elmaleh-Bergès, Monique, Ernault, Anais, Guilmin Crepon, Sophie, MCPH Consortium, Pirson, Isabelle, El Ghouzzi, Vincent, Auvin, Stéphane, Verloes, Alain, Passemard, Sandrine

المصدر: Developmental medicine and child neurology, 64 (4

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Adolescent, Ataxia, Cell Cycle Proteins -- genetics, Child, Preschool, Female, Humans, Intellectual Disability -- diagnosis -- genetics, Male, Microcephaly -- diagnosis -- genetics, Nerve Tissue Proteins -- genetics, Young Adult

وصف الملف: 2 full-text file(s): application/pdf | application/pdf

العلاقة: uri/info:doi/10.1111/dmcn.15060; uri/info:pmid/35726608; https://dipot.ulb.ac.be/dspace/bitstream/2013/356489/5/2021Ruaud.pdfTest; https://dipot.ulb.ac.be/dspace/bitstream/2013/356489/1/.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/356489Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/356489Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/356489/5/2021Ruaud.pdfTest
https://dipot.ulb.ac.be/dspace/bitstream/2013/356489/1/.pdfTest

المؤلفون: Christensen, Maria B., Levy, Amanda M., Mohammadi, Nazanin A., Niceta, Marcello, Kaiyrzhanov, Rauan, Dentici, Maria Lisa, Al Alam, Chadi, Alesi, Viola, Benoit, Valérie, Bhatia, Kailash P., Bierhals, Tatjana, Boßelmann, Christian M., Buratti, Julien, Callewaert, Bert, Ceulemans, Berten, Charles, Perrine, De Wachter, Matthias, Dehghani, Mohammadreza, D'haenens, Erika, Doco-Fenzy, Martine, Geßner, Michaela, Gobert, Cyrielle, Guliyeva, Ulviyya, Haack, Tobias B., Hammer, Trine B., Heinrich, Tilman, Hempel, Maja, Herget, Theresia, Hoffmann, Ute, Horvath, Judit, Houlden, Henry, Keren, Boris, Kresge, Christina, Kumps, Candy, Lederer, Damien, Lermine, Alban, Magrinelli, Francesca, Maroofian, Reza, Vahidi Mehrjardi, Mohammad Yahya, Moudi, Mahdiyeh, Müller, Amelie J., Oostra, Anna J., Pletcher, Beth A., Ros-Pardo, David, Samarasekera, Shanika, Tartaglia, Marco, Van Schil, Kristof, Vogt, Julie, Wassmer, Evangeline, Winkelmann, Juliane, Zaki, Maha S., Zech, Michael, Lerche, Holger, Radio, Francesca Clementina, Gomez-Puertas, Paulino, Møller, Rikke S., Tümer, Zeynep

المصدر: Christensen , M B , Levy , A M , Mohammadi , N A , Niceta , M , Kaiyrzhanov , R , Dentici , M L , Al Alam , C , Alesi , V , Benoit , V , Bhatia , K P , Bierhals , T , Boßelmann , C M , Buratti , J , Callewaert , B , Ceulemans , B , Charles , P , De Wachter , M , Dehghani , M , D'haenens , E , Doco-Fenzy , M , Geßner , M , Gobert , C , Guliyeva , U ....

مصطلحات موضوعية: epilepsy, intellectual disability, language impairement, movement disorder, neurodevelopmental disorder, ZNF142, Movement Disorders/complications, Phenotype, Humans, Intellectual Disability/diagnosis, Seizures/complications, Neurodevelopmental Disorders/genetics

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/b9666c14-0ee2-47fb-8f78-06ed69b80693Test

الإتاحة: https://doi.org/10.1111/cge.14165Test
https://portal.findresearcher.sdu.dk/da/publications/b9666c14-0ee2-47fb-8f78-06ed69b80693Test
https://findresearcher.sdu.dk/ws/files/203297012/Open_Access_Version.pdfTest

المؤلفون: Riggs, Erin Rooney, Bingaman, Taylor, Barry, Carrie-Ann, Behlmann, Andrea, Bluske, Krista, Bostwick, Bret, Bright, Alison, Chen, Chun-An, Clause, Amanda, Dharmadhikari, Avinash, Ganapathi, Mythily, Gonzaga-Jauregui, Claudia, Grant, Andrew, Hughes, Madeline, Kim, Se Rin, Krause, Amanda, Liao, Jun, Lumaka, Aimé, Mah, Michelle, Maloney, Caitlin, Mohan, Shruthi, Osei-Owusu, Ikeoluwa, Reble, Emma, Rennie, Olivia, Savatt, Juliann, Shimelis, Hermela, Siegert, Rebecca, Sneddon, Tam, Thaxton, Courtney, Toner, Kelly, Tran, Kien Trung, Webb, Ryan, Wilcox, Emma, Yin, Jiani, Zhuo, Xinming, Znidarsic, Masa, Martin, Christa Lese, Betancur, Catalina, Vorstman, Jacob A.S., Miller, David, Schaaf, Christian

المساهمون: Geisinger Autism & Developmental Medicine Institute Danville, PA, USA (ADMI), Drexel University, Invitae Corporation, Illumina, Baylor College of Medicine (BCM), Baylor University, Natera San Carlos, CA, USA, Children’s Hospital Los Angeles Los Angeles, Keck School of Medicine Los Angeles, University of Southern California (USC), Columbia University Irving Medical Center (CUIMC), Universidad Nacional Autónoma de México = National Autonomous University of Mexico (UNAM), Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School Boston (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital Boston, New York Medical College (NYMC), University of Illinois Chicago (UIC), University of Illinois System, National Human Genome Research Institute (NHGRI), University of the Witwatersrand Johannesburg (WITS), Université de Liège, Trillium Health Partners - Mississauga Hospital Mississauga, ON, Canada (THP-MH), University of Washington Seattle, University of North Carolina Chapel Hill (UNC), University of North Carolina System (UNC), St. Michael's Hospital, The Hospital for sick children Toronto (SickKids), Garvan Institute of medical research, Warren Alpert Medical School of Brown University, University of California Los Angeles (UCLA), University of California (UC), The Jackson Laboratory Bar Harbor (JAX), University Medical Centre Ljubljana Ljubljana, Slovenia (UMCL), Neuroscience Paris Seine (NPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Boston Children's Hospital, Harvard Medical School Boston (HMS), Heidelberg University Hospital Heidelberg, This work was supported by the National Human Genome Research Institute of the National Institutes of Health under award number U24HG006834.

المصدر: https://inserm.hal.science/inserm-03816347Test ; 2022, 24 (9), pp.1899-1908. ⟨10.1016/j.gim.2022.05.001⟩.

مصطلحات موضوعية: Autism, ClinGen, Gene–disease validity, Intellectual disability, Neurodevelopmental disorders, MESH: Autism Spectrum Disorder* / diagnosis, MESH: Autism Spectrum Disorder* / genetics, MESH: Autistic Disorder* / diagnosis, MESH: Autistic Disorder* / genetics, MESH: Humans, MESH: Intellectual Disability* / diagnosis, MESH: Intellectual Disability* / genetics, MESH: Neurodevelopmental Disorders* / genetics, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35616647; inserm-03816347; https://inserm.hal.science/inserm-03816347Test; https://inserm.hal.science/inserm-03816347/documentTest; https://inserm.hal.science/inserm-03816347/file/Riggs%20ClinGen%20ID%20autism%20Genet%20Med%202022.pdfTest; PUBMED: 35616647

الإتاحة: https://doi.org/10.1016/j.gim.2022.05.001Test
https://inserm.hal.science/inserm-03816347Test
https://inserm.hal.science/inserm-03816347/documentTest
https://inserm.hal.science/inserm-03816347/file/Riggs%20ClinGen%20ID%20autism%20Genet%20Med%202022.pdfTest

المؤلفون: Lubala, Toni Kasole, Kayembe-Kitenge, Tony, Mubungu, Gerrye, Lumaka Zola, Aimé, Kanteng, Gray, Savage, Sarah, Luboya, Oscar, Hagerman, Randi, Devriendt, Koenraad, Lukusa-Tshilobo, Prosper

المصدر: European Journal of Medical Genetics, 66 (9), 104819 (2023-09)

مصطلحات موضوعية: DR Congo, Face2Gene, Fragile X syndrome, Screening, Male, Adult, Female, Humans, Adolescent, Pilot Projects, Image Processing, Computer-Assisted, Fragile X Syndrome/diagnosis, Fragile X Syndrome/genetics, Intellectual Disability/diagnosis, Down Syndrome, Intellectual Disability, Genetics, Genetics (clinical), General Medicine, Human health sciences, Laboratory medicine & medical technology, Sciences de la santé humaine, Médecine de laboratoire & technologie médicale

العلاقة: https://api.elsevier.com/content/article/PII:S1769721223001258?httpAccept=text/xmlTest; urn:issn:1769-7212; urn:issn:1878-0849

الوصول الحر: https://orbi.uliege.be/handle/2268/307835Test

المؤلفون: Lebon, S., Quinodoz, M., Peter, V.G., Gengler, C., Blanchard, G., Cina, V., Campos-Xavier, B., Rivolta, C., Superti-Furga, A.

المصدر: Genes, vol. 12, no. 9, pp. 1397

مصطلحات موضوعية: Abortion, Eugenic, Agenesis of Corpus Callosum/complications, Agenesis of Corpus Callosum/diagnosis, Agenesis of Corpus Callosum/genetics, Child, Preschool, Developmental Disabilities/complications, Developmental Disabilities/genetics, Facial Asymmetry/complications, Facial Asymmetry/genetics, Family, Female, Fetal Diseases/diagnosis, Fetal Diseases/genetics, Heterozygote, Humans, Intellectual Disability/complications, Intellectual Disability/diagnosis, Intellectual Disability/genetics, Jumonji Domain-Containing Histone Demethylases/genetics, Mutation, Missense, Nuclear Proteins/genetics, Pedigree, Pregnancy, Repressor Proteins/genetics, Siblings, Switzerland, KDM5B

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34573379; info:eu-repo/semantics/altIdentifier/eissn/2073-4425; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_14ADEBC9C07B7; https://serval.unil.ch/notice/serval:BIB_14ADEBC9C07BTest; urn:issn:2073-4425; https://serval.unil.ch/resource/serval:BIB_14ADEBC9C07B.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_14ADEBC9C07B7Test

الإتاحة: https://doi.org/10.3390/genes12091397Test
https://serval.unil.ch/notice/serval:BIB_14ADEBC9C07BTest
https://serval.unil.ch/resource/serval:BIB_14ADEBC9C07B.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_14ADEBC9C07B7Test

المؤلفون: Erin Rooney Riggs, Taylor I. Bingaman, Carrie-Ann Barry, Andrea Behlmann, Krista Bluske, Bret Bostwick, Alison Bright, Chun-An Chen, Amanda R. Clause, Avinash V. Dharmadhikari, Mythily Ganapathi, Claudia Gonzaga-Jauregui, Andrew R. Grant, Madeline Y. Hughes, Se Rin Kim, Amanda Krause, Jun Liao, Aimé Lumaka, Michelle Mah, Caitlin M. Maloney, Shruthi Mohan, Ikeoluwa A. Osei-Owusu, Emma Reble, Olivia Rennie, Juliann M. Savatt, Hermela Shimelis, Rebecca K. Siegert, Tam P. Sneddon, Courtney Thaxton, Kelly A. Toner, Kien Trung Tran, Ryan Webb, Emma H. Wilcox, Jiani Yin, Xinming Zhuo, Masa Znidarsic, Christa Lese Martin, Catalina Betancur, Jacob A.S. Vorstman, David T. Miller, Christian P. Schaaf

المساهمون: Geisinger Autism & Developmental Medicine Institute [Danville, PA, USA] (ADMI), Drexel University, Invitae Corporation, Illumina, Baylor College of Medicine (BCM), Baylor University, Natera [San Carlos, CA, USA], Children’s Hospital Los Angeles [Los Angeles], Keck School of Medicine [Los Angeles], University of Southern California (USC), Columbia University Irving Medical Center (CUIMC), Universidad Nacional Autónoma de México = National Autonomous University of Mexico (UNAM), Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], New York Medical College (NYMC), University of Illinois [Chicago] (UIC), University of Illinois System, National Human Genome Research Institute (NHGRI), University of the Witwatersrand [Johannesburg] (WITS), Université de Liège, Trillium Health Partners - Mississauga Hospital [Mississauga, ON, Canada] (THP-MH), University of Washington [Seattle], University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC), St. Michael's Hospital, The Hospital for sick children [Toronto] (SickKids), Garvan Institute of medical research, Warren Alpert Medical School of Brown University, University of California [Los Angeles] (UCLA), University of California (UC), The Jackson Laboratory [Bar Harbor] (JAX), University Medical Centre Ljubljana [Ljubljana, Slovenia] (UMCL), Neuroscience Paris Seine (NPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Boston Children's Hospital, Harvard Medical School [Boston] (HMS), Heidelberg University Hospital [Heidelberg], This work was supported by the National Human Genome Research Institute of the National Institutes of Health under award number U24HG006834., Betancur, Catalina

المصدر: Genetics in Medicine
Genetics in Medicine, 2022, 24 (9), pp.1899-1908. ⟨10.1016/j.gim.2022.05.001⟩

مصطلحات موضوعية: ClinGen, MESH: Humans, Autism Spectrum Disorder, Autism, MESH: Autism Spectrum Disorder* / genetics, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, MESH: Autism Spectrum Disorder* / diagnosis, MESH: Intellectual Disability* / diagnosis, MESH: Intellectual Disability* / genetics, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Neurodevelopmental Disorders, Intellectual Disability, MESH: Autistic Disorder* / genetics, MESH: Autistic Disorder* / diagnosis, Humans, Autistic Disorder, MESH: Neurodevelopmental Disorders* / genetics, Genetics (clinical), Gene–disease validity

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b07ead00b13dfac939c5dc9322d918b8Test
https://doi.org/10.1016/j.gim.2022.05.001Test