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Open Accesshttps://doi.org/10.1136/jmedgenet-2017-105153
Copy DOI Journal: Journal of Medical Genetics |  Publication Date: Mar 21, 2018 |
 Citations: 12 |
Affiliation: Leiden University Medical Center, Sapienza University of Rome, The University of Texas Health Science Center at San Antonio, Université Côte d'Azur, Institute of Research on Cancer and Aging in Nice, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, University of Rochester Medical Center, Claude Bernard University Lyon 1, Laboratoire Interuniversitaire de Biologie de la Motricité, Jean Monnet University, Centre Hospitalier Universitaire de Saint-Étienne, Fred Hutch Cancer CenterBackground18p deletion syndrome is a rare disorder caused by partial or full monosomy of the short arm of chromosome 18. Clinical symptoms caused by 18p hemizygosity include cognitive impairment, mild...
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