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Autor:
El-Dessouky SH; Prenatal Diagnosis & Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Aboulghar MM; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Gaafar HM; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Abdella RM; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Sharaf MF; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Ateya MI; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Elarab AE; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Zidan WH; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Helal RM; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Aboelsaud SM; Fetal Medicine Unit, Cairo University, Cairo, Egypt., Eid MM; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Abdel-Salam GMH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Publikováno v:
Prenatal diagnosis [Prenat Diagn] 2020 Apr; Vol. 40 (5), pp. 565-576. Date of Electronic Publication: 2020 Feb 10.