Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

Autor: Ishorst, Nina1 (AUTHOR) e.mangold@uni.bonn.de, Henschel, Leonie1 (AUTHOR), Thieme, Frederic1 (AUTHOR), Drichel, Dmitriy2 (AUTHOR), Sivalingam, Sugirthan3,4,5 (AUTHOR), Mehrem, Sarah L.1 (AUTHOR), Fechtner, Ariane C.1 (AUTHOR), Fazaal, Julia1 (AUTHOR), Welzenbach, Julia1 (AUTHOR), Heimbach, André1 (AUTHOR), Maj, Carlo4 (AUTHOR), Borisov, Oleg4 (AUTHOR), Hausen, Jonas3,4,5 (AUTHOR), Raff, Ruth1 (AUTHOR), Hoischen, Alexander6,7,8 (AUTHOR), Dixon, Michael9 (AUTHOR), Rada‐Iglesias, Alvaro10 (AUTHOR), Bartusel, Michaela11,12 (AUTHOR), Rojas‐Martinez, Augusto13,14 (AUTHOR), Aldhorae, Khalid15,16 (AUTHOR)
Zdroj: Molecular Genetics & Genomic Medicine. Mar2023, Vol. 11 Issue 3, p1-16. 16p.
Databáze: Academic Search Ultimate
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