Delineation of the clinical phenotype caused by de novo CLTC variants
MJ Nabais Sa,H Venselaar,L Wiel,A Trimouille,E Lasseaux,S Naudion,D Lacombe,A Piton,C Vincent-Delorme,C Zweier,A Reis, R Trollmann,A Ruiz,E Gabau,A Vetro,R Guerrini,S Bakhtiari,M Kruer, K Crompton,DJ Amor,EK Bijlsma,TS Barakat, MF van Dooren,R Pfundt,C Gilissen,BB de Vries, AP de Brouwer,DA Koolen EUROPEAN JOURNAL OF HUMAN GENETICS(2019)
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