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المؤلفون: Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C. Y. Loo, Lauren A. Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S. Moldenhauer, Anne S. Bassett, Donna M. McDonald-McGinn
المصدر: Genes; Volume 14; Issue 1; Pages: 160
مصطلحات موضوعية: Male, Heart Defects, Congenital, prenatal ultrasound, fetal cardiac anomaly, Fetal Diseases, Pregnancy, 22q11.2 deletion syndrome, noninvasive prenatal screening, preimplantation genetic testing, Prenatal Diagnosis, Genetics, DiGeorge Syndrome, Humans, Female, Genetic Testing, Child, Genetics (clinical)
وصف الملف: Electronic; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeda4822e813a946213fec47cb722e03Test
https://lirias.kuleuven.be/handle/20.500.12942/714720Test -
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المؤلفون: Wolfram Demaerel, Matthew S. Hestand, Elfi Vergaelen, Ann Swillen, Marcos López-Sánchez, Luis A. Pérez-Jurado, Donna M. McDonald-McGinn, Elaine Zackai, Beverly S. Emanuel, Bernice E. Morrow, Jeroen Breckpot, Koenraad Devriendt, Joris R. Vermeesch, Kevin Antshel, Celso Arango, Marco Armando, Anne Bassett, Carrie Bearden, Erik Boot, Marta Bravo-Sanchez, Elemi Breetvelt, Tiffany Busa, Nancy Butcher, Linda Campbell, Miri Carmel, Eva Chow, T. Blaine Crowley, Joseph Cubells, David Cutler, Maria Cristina Digilio, Sasja Duijff, Stephan Eliez, Beverly Emanuel, Michael Epstein, Rens Evers, Luis Fernandez Garcia-Moya, Ania Fiksinski, David Fraguas, Wanda Fremont, Rosemarie Fritsch, Sixto Garcia-Minaur, Aaron Golden, Doron Gothelf, Tingwei Guo, Ruben Gur, Raquel Gur, Damian Heine-Suner, Matthew Hestand, Stephen Hooper, Wendy Kates, Leila Kushan, Alejandra Laorden-Nieto, Johanna Maeder, Bruno Marino, Christian Marshall, Kathryn McCabe, Donna McDonald-McGinn, Elena Michaelovosky, Bernice Morrow, Edward Moss, Jennifer Mulle, Declan Murphy, Kieran Murphy, Clodagh Murphy, Maria Niarchou, Claudia Ornstein, Michael Owen, Nicole Philip, Gabriela Repetto, Maude Schneider, Vandana Shashi, Tony Simon, Flora Tassone, Marta Unolt, Therese van Amelsvoort, Marianne van den Bree, Esther Van Duin, Joris Vermeesch, Stefano Vicari, Claudia Vingerhoets, Jacob Vorstman, Steve Warren, Ronnie Weinberger, Omri Weisman, Abraham Weizman, Zhengdong Zhang, Michael Zwick
المصدر: The American Journal of Human Genetics. 103:457
مصطلحات موضوعية: Genetics, DNA Copy Number Variations, Notice, Chromosome, Locus (genetics), Inversion (meteorology), Biology, Polymorphism, Single Nucleotide, Genome, Human genetics, Retraction, Meiosis, Polymorphism (computer science), Report, Chromosome Inversion, DiGeorge Syndrome, Humans, Genetic Predisposition to Disease, Chromosome Deletion, Homologous Recombination, In Situ Hybridization, Fluorescence, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d117da35c3a2f68c69992a1cff22be9aTest
https://doi.org/10.1016/j.ajhg.2018.08.011Test