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Maha M Eid

Showing results (1-10 of 31) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 23, 2018
A Homozygous Missense Mutation in FANCA Gene in a 46,XY Female with Gonadal DysgenesisInas Mazen, Kenneth McElreavey, Maha M Eid, et al.
Prenatal Diagnosis|August 15, 2020
Response to letter from Okoye JO and Ngokere AA "Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?"Ghada M H Abdel-Salam, Sara H El-Dessouky, Mona M Aboulghar, et al.
Pediatric Dermatology|June 23, 2011
Ectodermal abnormalities in patients with Kabuki syndromeGhada M H Abdel-Salam, Hanan H Afifi, Maha M Eid, et al.
Pediatric Dermatology|February 13, 2016
De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features DisorderHanan H Afifi, Mohamed S Abdel-Hamid, Maha M Eid, et al.
Reproductive Biology|March 3, 2020
Detection of low-grade mosaicism and its correlation with hormonal profile, testicular volume, and semen quality in a cohort of Egyptian Klinefelter and Klinefelter-like patientsAbdelrahman Madian, Maha M Eid, Adel A B Shahin, et al.
Journal of Human Genetics|July 27, 2022
A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasiaGhada M H Abdel-Salam, Marian Girgis, Maha M Eid, 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.
Journal of Pediatric Genetics|July 28, 2020
Clinical Variability of Pallister-Killian Syndrome in Two Egyptian PatientsMaha M Eid, Ola M Eid, Sawsan Abdel-Hadi, et al.
Journal of Pediatric Genetics|January 16, 2023
Erratum: Clinical Variability of Pallister-Killian Syndrome in Two Egyptian PatientsMaha M Eid, Ola M Eid, Sawsan Abdel-Hadi, et al.
Journal, Genetic Engineering & Biotechnology|June 28, 2021
Evaluation of MLPA as a comprehensive molecular cytogenetic tool to detect cytogenetic markers of chronic lymphocytic leukemia in Egyptian patientsOla M Eid, Rania M A Abdel Kader, Lamiaa A Fathalla, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 23, 2018
A Homozygous Missense Mutation in FANCA Gene in a 46,XY Female with Gonadal DysgenesisInas Mazen, Kenneth McElreavey, Maha M Eid, et al.
Prenatal Diagnosis|August 15, 2020
Response to letter from Okoye JO and Ngokere AA "Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?"Ghada M H Abdel-Salam, Sara H El-Dessouky, Mona M Aboulghar, et al.
Pediatric Dermatology|June 23, 2011
Ectodermal abnormalities in patients with Kabuki syndromeGhada M H Abdel-Salam, Hanan H Afifi, Maha M Eid, et al.
Pediatric Dermatology|February 13, 2016
De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features DisorderHanan H Afifi, Mohamed S Abdel-Hamid, Maha M Eid, et al.
Reproductive Biology|March 3, 2020
Detection of low-grade mosaicism and its correlation with hormonal profile, testicular volume, and semen quality in a cohort of Egyptian Klinefelter and Klinefelter-like patientsAbdelrahman Madian, Maha M Eid, Adel A B Shahin, et al.
Journal of Human Genetics|July 27, 2022
A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasiaGhada M H Abdel-Salam, Marian Girgis, Maha M Eid, 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.
Journal of Pediatric Genetics|July 28, 2020
Clinical Variability of Pallister-Killian Syndrome in Two Egyptian PatientsMaha M Eid, Ola M Eid, Sawsan Abdel-Hadi, et al.
Journal of Pediatric Genetics|January 16, 2023
Erratum: Clinical Variability of Pallister-Killian Syndrome in Two Egyptian PatientsMaha M Eid, Ola M Eid, Sawsan Abdel-Hadi, et al.
Journal, Genetic Engineering & Biotechnology|June 28, 2021
Evaluation of MLPA as a comprehensive molecular cytogenetic tool to detect cytogenetic markers of chronic lymphocytic leukemia in Egyptian patientsOla M Eid, Rania M A Abdel Kader, Lamiaa A Fathalla, et al.
Pageof 4