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Rare deleterious mutations of HNRNP genes result in shared ..:
Gillentine, Madelyn A
;
Wang, Tianyun
;
Hoekzema, Kendra
...
qt9ff2t46d. , 2021
Link:
https://escholarship.org/uc/item/9ff2t46d
RT Journal T1
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt9ff2t46d&Exemplar=1&LAN=DE A1 Gillentine, Madelyn A A1 Wang, Tianyun A1 Hoekzema, Kendra A1 Rosenfeld, Jill A1 Liu, Pengfei A1 Guo, Hui A1 Kim, Chang N A1 De Vries, Bert BA A1 Vissers, Lisenka ELM A1 Nordenskjold, Magnus A1 Kvarnung, Malin A1 Lindstrand, Anna A1 Nordgren, Ann A1 Gecz, Jozef A1 Iascone, Maria A1 Cereda, Anna A1 Scatigno, Agnese A1 Maitz, Silvia A1 Zanni, Ginevra A1 Bertini, Enrico A1 Zweier, Christiane A1 Schuhmann, Sarah A1 Wiesener, Antje A1 Pepper, Micah A1 Panjwani, Heena A1 Torti, Erin A1 Abid, Farida A1 Anselm, Irina A1 Srivastava, Siddharth A1 Atwal, Paldeep A1 Bacino, Carlos A A1 Bhat, Gifty A1 Cobian, Katherine A1 Bird, Lynne M A1 Friedman, Jennifer A1 Wright, Meredith S A1 Callewaert, Bert A1 Petit, Florence A1 Mathieu, Sophie A1 Afenjar, Alexandra A1 Christensen, Celenie K A1 White, Kerry M A1 Elpeleg, Orly A1 Berger, Itai A1 Espineli, Edward J A1 Fagerberg, Christina A1 Brasch-Andersen, Charlotte A1 Hansen, Lars Kjærsgaard A1 Feyma, Timothy A1 Hughes, Susan A1 Thiffault, Isabelle A1 Sullivan, Bonnie A1 Yan, Shuang A1 Keller, Kory A1 Keren, Boris A1 Mignot, Cyril A1 Kooy, Frank A1 Meuwissen, Marije A1 Basinger, Alice A1 Kukolich, Mary A1 Philips, Meredith A1 Ortega, Lucia A1 Drummond-Borg, Margaret A1 Lauridsen, Mathilde A1 Sorensen, Kristina A1 Lehman, Anna A1 Lopez-Rangel, Elena A1 Levy, Paul A1 Lessel, Davor A1 Lotze, Timothy A1 Madan-Khetarpal, Suneeta A1 Sebastian, Jessica A1 Vento, Jodie A1 Vats, Divya A1 Benman, L Manace A1 Mckee, Shane A1 Mirzaa, Ghayda M A1 Muss, Candace A1 Pappas, John A1 Peeters, Hilde A1 Romano, Corrado A1 Elia, Maurizio A1 Galesi, Ornella A1 Simon, Marleen EH A1 van Gassen, Koen LI A1 Simpson, Kara A1 Stratton, Robert A1 Syed, Sabeen A1 Thevenon, Julien A1 Palafoll, Irene Valenzuela A1 Vitobello, Antonio A1 Bournez, Marie A1 Faivre, Laurence A1 Xia, Kun A1 Earl, Rachel K A1 Nowakowski, Tomasz A1 Bernier, Raphael A A1 Eichler, Evan E PB eScholarship, University of California YR 2021 K1 Biotechnology K1 Human Genome K1 Genetics K1 Genetic Testing K1 Brain Disorders K1 Neurosciences K1 Pediatric K1 Aetiology K1 2.1 Biological and endogenous factors K1 Brain K1 DNA Copy Number Variations K1 Gene Expression Regulation K1 Genetic Association Studies K1 Genetic Predisposition to Disease K1 Genetic Variation K1 Heterogeneous-Nuclear Ribonucleoproteins K1 Humans K1 Inheritance Patterns K1 Mutation K1 Missense K1 Neurodevelopmental Disorders K1 Phenotype K1 RNA Processing K1 Post-Transcriptional K1 Single-Cell Analysis K1 hnRNPs K1 Cortex development K1 Gene families K1 CAUSES Study K1 SPARK Consortium K1 Clinical Sciences JF qt9ff2t46d LK http://dx.doi.org/https://escholarship.org/uc/item/9ff2t46d DO https://escholarship.org/uc/item/9ff2t46d SF ELIB - SuUB Bremen
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