RETRACTED: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements

Author:

Demaerel Wolfram,Hestand Matthew S.,Vergaelen Elfi,Swillen Ann,López-Sánchez Marcos,Pérez-Jurado Luis A.,McDonald-McGinn Donna M.,Zackai Elaine,Emanuel Beverly S.,Morrow Bernice E.,Breckpot Jeroen,Devriendt Koenraad,Vermeesch Joris R.,Antshel Kevin,Arango Celso,Armando Marco,Bassett Anne,Bearden Carrie,Boot Erik,Bravo-Sanchez Marta,Breetvelt Elemi,Busa Tiffany,Butcher Nancy,Campbell Linda,Carmel Miri,Chow Eva,Crowley T. Blaine,Cubells Joseph,Cutler David,Demaerel Wolfram,Digilio Maria Cristina,Duijff Sasja,Eliez Stephan,Emanuel Beverly,Epstein Michael,Evers Rens,Fernandez Garcia-Moya Luis,Fiksinski Ania,Fraguas David,Fremont Wanda,Fritsch Rosemarie,Garcia-Minaur Sixto,Golden Aaron,Gothelf Doron,Guo Tingwei,Gur Ruben,Gur Raquel,Heine-Suner Damian,Hestand Matthew,Hooper Stephen,Kates Wendy,Kushan Leila,Laorden-Nieto Alejandra,Maeder Johanna,Marino Bruno,Marshall Christian,McCabe Kathryn,McDonald-McGinn Donna,Michaelovosky Elena,Morrow Bernice,Moss Edward,Mulle Jennifer,Murphy Declan,Murphy Kieran,Murphy Clodagh,Niarchou Maria,Ornstein Claudia,Owen Michael,Philip Nicole,Repetto Gabriela,Schneider Maude,Shashi Vandana,Simon Tony,Swillen Ann,Tassone Flora,Unolt Marta,van Amelsvoort Therese,van den Bree Marianne,Van Duin Esther,Vergaelen Elfi,Vermeesch Joris,Vicari Stefano,Vingerhoets Claudia,Vorstman Jacob,Warren Steve,Weinberger Ronnie,Weisman Omri,Weizman Abraham,Zackai Elaine,Zhang Zhengdong,Zwick Michael

Funder

IWT

KUL

FWO

National Institute of Mental Health

Belgian Science Policy Office Interuniversity Attraction Poles

Marató de TV3

Spanish Ministry of Economy and Competitiveness

Catalan Department of Economy and Knowledge

Jerome Lejeune Foundation

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference51 articles.

1. The annual incidence of DiGeorge/velocardiofacial syndrome;Devriendt;J. Med. Genet.,1998

2. 22q11.2 deletion syndrome;McDonald-McGinn;Nat Rev Dis Primers,2015

3. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies;Grati;Prenat. Diagn.,2015

4. Developmental trajectories in 22q11.2 deletion;Swillen;Am. J. Med. Genet. C. Semin. Med. Genet.,2015

5. 22q11 deletion syndrome: a genetic subtype of schizophrenia;Bassett;Biol. Psychiatry,1999

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