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Sara H El-Dessouky

Showing results (1-10 of 16) with videos related to

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Neurogenetics|August 2, 2021
Fetal brain arrest broadens the spectrum of WDR81-related developmental brain malformationsMohamed S Abdel-Hamid, Sahar Sabry, Sherif F Abdel-Ghafar, et al.
American Journal of Medical Genetics. Part A|January 15, 2019
Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephalyMohamed S Abdel-Hamid, Sara H El-Dessouky, Mohamed I Ateya, et al.
Clinical Genetics|January 7, 2025
Lethal Phenotype and Expansion of the Clinical Spectrum of Biallelic Loss of Function Variant in SENP7 Gene Unveiled by Whole Exome SequencingAhmed K Saad, Nagwa H Hassan, Hala N Soliman, et al.
Molecular Genetics and Genomics : MGG|March 12, 2022
Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effectManal M Thomas, Heba Mostafa Ahmed, Sara H El-Dessouky, et al.
Journal, Genetic Engineering & Biotechnology|July 28, 2022
MLPA as a genetic assay for the prenatal diagnosis of common aneuploidy: the first Egyptian experienceOla M Eid, Maha M Eid, Marwa Farid, et al.
American Journal of Medical Genetics. Part A|September 10, 2020
Prenatal delineation of a distinct lethal fetal syndrome caused by a homozygous truncating KIDINS220 variantSara H El-Dessouky, Mahmoud Y Issa, Mona M Aboulghar, et al.
Prenatal Diagnosis|August 25, 2020
Raine syndrome: Prenatal diagnosis based on recognizable fetal facial features and characteristic intracranial calcificationSara H El-Dessouky, Mohamed S Abdel-Hamid, Sherif F Abdel-Ghafar, et al.
Biology of Reproduction|December 27, 2025
Loss of the Maternal Effect Gene NLRP2 Impairs Embryonic and Extra-Embryonic Development, Revealing a Novel Genetic Cause of Congenital Anomalies†Momal Sharif, Zahra Anvar, Imen Chakchouk, et al.
Journal of Perinatal Medicine|September 9, 2019
Fetal heart examination at the time of 13 weeks scan: a 5 years' prospective studyAlaa Ebrashy, Mona Aboulghar, Mohamed Elhodiby, et al.
Prenatal Diagnosis|January 20, 2020
Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associationsSara H El-Dessouky, Mona M Aboulghar, Hassan M Gaafar, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Neurogenetics|August 2, 2021
Fetal brain arrest broadens the spectrum of WDR81-related developmental brain malformationsMohamed S Abdel-Hamid, Sahar Sabry, Sherif F Abdel-Ghafar, et al.
American Journal of Medical Genetics. Part A|January 15, 2019
Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephalyMohamed S Abdel-Hamid, Sara H El-Dessouky, Mohamed I Ateya, et al.
Clinical Genetics|January 7, 2025
Lethal Phenotype and Expansion of the Clinical Spectrum of Biallelic Loss of Function Variant in SENP7 Gene Unveiled by Whole Exome SequencingAhmed K Saad, Nagwa H Hassan, Hala N Soliman, et al.
Molecular Genetics and Genomics : MGG|March 12, 2022
Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effectManal M Thomas, Heba Mostafa Ahmed, Sara H El-Dessouky, et al.
Journal, Genetic Engineering & Biotechnology|July 28, 2022
MLPA as a genetic assay for the prenatal diagnosis of common aneuploidy: the first Egyptian experienceOla M Eid, Maha M Eid, Marwa Farid, et al.
American Journal of Medical Genetics. Part A|September 10, 2020
Prenatal delineation of a distinct lethal fetal syndrome caused by a homozygous truncating KIDINS220 variantSara H El-Dessouky, Mahmoud Y Issa, Mona M Aboulghar, et al.
Prenatal Diagnosis|August 25, 2020
Raine syndrome: Prenatal diagnosis based on recognizable fetal facial features and characteristic intracranial calcificationSara H El-Dessouky, Mohamed S Abdel-Hamid, Sherif F Abdel-Ghafar, et al.
Biology of Reproduction|December 27, 2025
Loss of the Maternal Effect Gene NLRP2 Impairs Embryonic and Extra-Embryonic Development, Revealing a Novel Genetic Cause of Congenital Anomalies†Momal Sharif, Zahra Anvar, Imen Chakchouk, et al.
Journal of Perinatal Medicine|September 9, 2019
Fetal heart examination at the time of 13 weeks scan: a 5 years' prospective studyAlaa Ebrashy, Mona Aboulghar, Mohamed Elhodiby, et al.
Prenatal Diagnosis|January 20, 2020
Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associationsSara H El-Dessouky, Mona M Aboulghar, Hassan M Gaafar, et al.
Pageof 2