A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome
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Published:2020-06-01
Issue:10
Volume:28
Page:1422-1431
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ISSN:1018-4813
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Container-title:European Journal of Human Genetics
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language:en
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Short-container-title:Eur J Hum Genet
Author:
Drivas Theodore G., Li Dong, Nair Divya, Alaimo Joseph T., Alders Mariëlle, Altmüller Janine, Barakat Tahsin StefanORCID, Bebin E. Martina, Bertsch Nicole L., Blackburn Patrick R.ORCID, Blesson Alyssa, Bouman Arjan M., Brockmann Knut, Brunelle Perrine, Burmeister MargitORCID, Cooper Gregory M.ORCID, Denecke Jonas, Dieux-Coëslier Anne, Dubbs Holly, Ferrer AlejandroORCID, Gal Danna, Bartik Lauren E., Gunderson Lauren B., Hasadsri Linda, Jain Mahim, Karimov Catherine, Keena Beth, Klee Eric W., Kloth Katja, Lace Baiba, Macchiaiolo Marina, Marcadier Julien L., Milunsky Jeff M., Napier Melanie P., Ortiz-Gonzalez Xilma R., Pichurin Pavel N., Pinner Jason, Powis ZoeORCID, Prasad Chitra, Radio Francesca ClementinaORCID, Rasmussen Kristen J.ORCID, Renaud Deborah L., Rush Eric T., Saunders Carol, Selcen Duygu, Seman Ann R., Shinde Deepali N., Smith Erica D.ORCID, Smol ThomasORCID, Snijders Blok Lot, Stoler Joan M., Tang Sha, Tartaglia Marco, Thompson Michelle L., van de Kamp Jiddeke M., Wang Jingmin, Weise Dagmar, Weiss Karin, Woitschach Rixa, Wollnik Bernd, Yan HuifangORCID, Zackai Elaine H., Zampino Giuseppe, Campeau PhilippeORCID, Bhoj Elizabeth
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Cited by
28 articles.
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