Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort.
El-Dessouky SH, Sharaf-Eldin WE, Aboulghar MM, Mousa HA, Zaki MS, Maroofian R, Senousy SM, Eid MM, Gaafar HM, Ebrashy A, Shikhah AZ, Abdelfattah AN, Ezz-Elarab A, Ateya MI, Hosny A, Youssef MA, Abdella R, Issa MY, Matsa LS, Abdelaziz N, Saad AK, Alavi S, Tajsharghi H, Abdalla EM.
El-Dessouky SH, et al. Among authors: mousa ha.
Clin Genet. 2025 Jul;108(1):33-48. doi: 10.1111/cge.14712. Epub 2025 Jan 31.
Clin Genet. 2025.
PMID: 39891418