LHX2 haploinsufficiency causes a variable neurodevelopmental disorder
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Published:2023-07
Issue:7
Volume:25
Page:100839
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Schmid Cosima M., Gregor Anne, Costain Gregory, Morel Chantal F., Massingham Lauren, Schwab Jennifer, Quélin Chloé, Faoucher Marie, Kaplan Julie, Procopio Rebecca, Saunders Carol J., Cohen Ana S.A., Lemire Gabrielle, Sacharow Stephanie, O’Donnell-Luria Anne, Segal Ranit Jaron, Kianmahd Shamshoni Jessica, Schweitzer Daniela, Ebrahimi-Fakhari Darius, Monaghan Kristin, Palculict Timothy Blake, Napier Melanie P., Tao Alice, Isidor Bertrand, Moradkhani Kamran, Reis André, Sticht Heinrich, Chung Wendy K., Zweier ChristianeORCID
Subject
Genetics (clinical)
Cited by
5 articles.
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