Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect.
El-Dessouky SH, Sharaf-Eldin WE, Aboulghar MM, Ebrashy A, Senousy SM, Elarab AE, Gaafar HM, Ateya MI, Abdelfattah AN, Saad AK, Zolfokar DS, Fouad MM, Abdella RM, Sharaf MF, Issa MY, Matsa LS, Aref H, Soliman SH, Al-Bellehy MA, Abdel-Aziz NN, ElHodiby ME, Abdou HK, Eid MM, Zaki MS, Abdalla EM.
El-Dessouky SH, et al. Among authors: eid mm.
Prenat Diagn. 2024 Dec 5. doi: 10.1002/pd.6697. Online ahead of print.
Prenat Diagn. 2024.
PMID: 39638571