Autor/in Chopra, Maya 1 Clayton-Smith, Jill 1 Girisha, Katta M 1 Kaur, Anupriya 1 Kaur, Parneet 1 Mancini, Grazia M S McEntagart, Meriel Pfundt, Rolph 1 Platzer, Konrad 1 Shukla, Anju Veenstra-Knol, Hermine 1 alle zeigenListe einklappen
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism Chopra, Maya McEntagart, Meriel Clayton-Smith, Jill Platzer, Konrad Shukla, Anju Girisha, Katta M Kaur, Anupriya 2021 - Forschungsinformationssystem des UKE
