DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations
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Published:2024-07
Issue:7
Volume:26
Page:101126
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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:
Lavillaureix Alinoë, Rollier Paul, Kim Artem, Panasenkava Veranika, De Tayrac Marie, Carré Wilfrid, Guyodo Hélène, Faoucher Marie, Poirel Elisabeth, Akloul Linda, Quélin Chloé, Whalen Sandra, Bos Jessica, Broekema Marjoleine, van Hagen Johanna M., Grand Katheryn, Allen-Sharpley Michelle, Magness Emily, McLean Scott D., Kayserili Hülya, Altunoglu Umut, En Qi Chong Angie, Xue Shifeng, Jeanne Médéric, Almontashiri Naif, Habhab Wisam, Vanlerberghe Clemence, Faivre Laurence, Viora-Dupont Eléonore, Philippe Christophe, Safraou Hana, Laffargue Fanny, Mittendorf Luisa, Abou Jamra Rami, Patil Siddaramappa Jagdish, Dalal Ashwin, Sarma Asodu Sandeep, Keren Boris, Reversade Bruno, Dubourg Christèle, Odent Sylvie, Dupé ValérieORCID
Funder
Centre Hospitalier Universitaire de Rennes ANR
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