المؤلفون: Agrawal, Pankaj, Armstrong Scott, Daryl, Barkoudah, Elizabeth, Bellini, Melissa, Beneteau, Claire, Bjørgo, Kathrine, Brooks, Alice, Brown, Natasha, Castle, Alison, Castro, Diana, Chorin, Odelia, Cleghorn, Mark, Clement, Emma, Coman, David, Costin, Carrie, Devriendt, Koen, Dong, Dexin, Dries, Annika, Duelund Hjortshøj, Tina, Dyment, David, Eng, Christine, Genetti, Casie, Grano, Siera, Henneman, Peter, Heron, Delphine, Hoffmann, Katrin, Hom, Jason, Du, Haowei, Iascone, Maria, Isidor, Bertrand, Järvelä, Irma E., Jones, Julie, Keren, Boris, Koenig, Mary Kay, Kohlhase, Jürgen, Lalani, Seema, Le Caignec, Cedric, Lewis, Andi, Liu, Pengfei, Lovgren, Alysia, Lupski, James R., Lyons, Mike, Lysy, Philippe, Manning, Melanie, Marcelis, Carlo, McLean, Scott Douglas, Mercie, Sandra, Mertens, Mareike, Molin, Arnaud, Nizon, Mathilde, Nugent, Kimberly Margaret, Öhman, Susanna, O'Leary, Melanie, Okashah Littlejohn, Rebecca, Petit, Florence, Pfundt, Rolph, Pottocki, Lorraine, Raas-Rotschild, Annick, Ranguin, Kara, Revencu, Nicole, Rosenfeld, Jill, Rhodes, Lindsay, Santos Simmaro, Fernando, Sals, Karen, Schieving, Jolanda, Schrauwen, Isabelle, Schuurs-Hoeijmakers, Janneke H.M., Seaby, Eleanor G., Sheffer, Ruth, Snijders Blok, Lot, Sørensen, Kristina P., Srivastava, Siddharth, Stark, Zornitza, Stoeva, Radka, Stutterd, Chloe, Tan, Natalie B., Mathiesen Torring, Pernille, Vanakker, Olivier, van der Laan, Liselot, Ververi, Athina, Villavicencio-Lorini, Pablo, Vincent, Marie, Wand, Dorothea, Wessels, Marja, White, Sue, Wojcik, Monica H., Wu, Nan, Zhao, Sen, Pérez Baca, María del Rocío, Jacobs, Eva Z., Vantomme, Lies, Leblanc, Pontus, Bogaert, Elke, Dheedene, Annelies, De Cock, Laurenz, Haghshenas, Sadegheh, Foroutan, Aidin, Levy, Michael A., Kerkhof, Jennifer, McConkey, Haley, Chen, Chun-An, Batzir, Nurit Assia, Wang, Xia, Palomares, María, Carels, Marieke, Dermaut, Bart, Sadikovic, Bekim, Menten, Björn, Yuan, Bo, Vergult, Sarah, Callewaert, Bert

المصدر: In The American Journal of Human Genetics 7 March 2024 111(3):509-528

المؤلفون: Kristensen, Steffen Ernesto, Kvist Ekelund, Charlotte, Sandager, Puk, Stener Jørgensen, Finn, Hoseth, Eva, Sperling, Lene, Zingenberg, Helle Jeanette, Duelund Hjortshøj, Tina, Gadsbøll, Kasper, Wright, Alan, Wright, David, McLennan, Andrew, Sundberg, Karin, Petersen, Olav Bjørn

المصدر: In American Journal of Obstetrics and Gynecology November 2023 229(5):555-555

المؤلفون: Kristensen, Steffen Ernesto, Ekelund, Charlotte Kvist, Sandager, Puk, Jørgensen, Finn Stener, Hoseth, Eva, Sperling, Lene, Zingenberg, Helle Jeanette, Duelund Hjortshøj, Tina, Gadsbøll, Kasper, Wright, Alan, Wright, David, McLennan, Andrew, Sundberg, Karin, Petersen, Olav Bjørn

المصدر: Kristensen , S E , Ekelund , C K , Sandager , P , Jørgensen , F S , Hoseth , E , Sperling , L , Zingenberg , H J , Duelund Hjortshøj , T , Gadsbøll , K , Wright , A , Wright , D , McLennan , A , Sundberg , K & Petersen , O B 2023 , ' Triple trouble : uncovering the risks and benefits of early fetal reduction in trichorionic triplets in a large national Danish cohort study ' , American Journal of Obstetrics and Gynecology , vol. 229 , no. 5 , pp. 555.e1-555.e14 .

مصطلحات الفهرس: adverse pregnancy outcome, chance of live born, Danish national cohort, embryo reduction, multifetal pregnancy, multifetal pregnancy reduction, multiples, pregnancy complications, preterm birth, preterm delivery, reproductive autonomy, selective termination, article

URL: https://curis.ku.dk/portal/da/publications/triple-trouble(ec4b1e01-2915-43fe-a283-e67d2ee8748c).html
https://doi.org/10.1016/j.ajog.2023.05.029
https://curis.ku.dk/ws/files/374831818/1_s2.0_S0002937823003678_main.pdf

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المؤلفون: Wolfe, Kate, McQuillin, Andrew, Alesi, Viola, Boudry Labis, Elise, Cutajar, Peter, Dallapiccola, Bruno, Dentici, Maria Lisa, Dieux-Coeslier, Anne, Duban-Bedu, Benedicte, Duelund Hjortshøj, Tina, Goel, Himanshu, Loddo, Sara, Morrogh, Deborah, Mosca-Boidron, Anne-Laure, Novelli, Antonio, Olivier-Faivre, Laurence, Parker, Jennifer, Parker, Michael J, Patch, Christine, Pelling, Anna L, Smol, Thomas, Tümer, Zeynep, Vanakker, Olivier, van Haeringen, Arie, Vanlerberghe, Clémence, Strydom, Andre, Skuse, David, Bass, Nick

المصدر: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Wolfe, K, McQuillin, A, Alesi, V, Boudry Labis, E, Cutajar, P, Dallapiccola, B, Dentici, M L, Dieux-Coeslier, A, Duban-Bedu, B, Duelund Hjortshøj, T, Goel, H, Loddo, S, Morrogh, D, Mosca-Boidron, A-L, Novelli, A, Olivier-Faivre, L, Parker, J, Parker, M J, Patch, C, Pelling, A L, Smol, T, Tümer, Z, Vanakker, O, van Haeringen, A, Vanlerberghe, C, Strydom, A, Skuse, D & Bass, N 2018, ' Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 177, no. 4, pp. 397-405 . https://doi.org/10.1002/ajmg.b.32627

مصطلحات موضوعية: Adult, Male, INTELLECTUAL DISABILITY, Adolescent, DNA Copy Number Variations, DISORDERS, autism spectrum disorders, Developmental Disabilities, Gene Duplication, Intellectual Disability, SCHIZOPHRENIA, Chromosome Duplication, Medicine and Health Sciences, Humans, VALIDITY, AUTISM, Child, COPY-NUMBER VARIANTS, Chromosome Aberrations, DEVELOPMENTAL DELAY, Mental Disorders, Biology and Life Sciences, United Kingdom, INDIVIDUALS, attention deficit hyperactivity disorder, Phenotype, Child, Preschool, Chromosomes, Human, Pair 2, RELIABILITY, Female, intellectual disabilities, Chromosome Deletion, copy number variants

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0886505d8cd68a4e46337a6df881e3dd
https://pubmed.ncbi.nlm.nih.gov/29603867