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Maha M Eid

Showing results (11-20 of 31) with videos related to

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Cytogenetic and Genome Research|November 13, 2019
Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic FeaturesMaha S Zaki, Ola M Eid, Maha M Eid, et al.
The Gulf Journal of Oncology|October 12, 2017
Evaluation of BRCA1 Large Genomic Rearrangements in Group of Egyptian Female Breast Cancer Patients Using MLPAOla M Eid, Eman A El Ghoroury, Maha M Eid, et al.
Current Pharmaceutical Biotechnology|March 21, 2020
Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic AberrationsHanaa R M Attia, Amany H Abdelrahman, Mona H Ibrahim, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotypeGhada M H Abdel-Salam, Laura Flores-Sarnat, Mona O El-Ruby, et al.
Congenital Anomalies|December 30, 2015
Expanding the mutation and clinical spectrum of Roberts syndromeHanan H Afifi, Ghada M H Abdel-Salam, Maha M Eid, et al.
Cytogenetic and Genome Research|March 19, 2020
Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-InactivationAmal M Mohamed, Maha M Eid, Ola M Eid, et al.
Journal of Pediatric Urology|December 19, 2012
Anti-diuretic hormone and genetic study in primary nocturnal enuresisAmany A A Fatouh, Ayat A Motawie, Amany M Abd Al-Aziz, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndromeNoriko Miyake, Ghada Abdel-Salam, Takanori Yamagata, et al.
Journal, Genetic Engineering & Biotechnology|November 10, 2023
Detection of AZFc gene deletion in a cohort of Egyptian patients with idiopathic male infertilityMaha M Eid, Ola M Eid, Amany H Abdelrahman, et al.
American Journal of Medical Genetics. Part A|October 13, 2011
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorderGhada M H Abdel-Salam, Noriko Miyake, Maha M Eid, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Cytogenetic and Genome Research|November 13, 2019
Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic FeaturesMaha S Zaki, Ola M Eid, Maha M Eid, et al.
The Gulf Journal of Oncology|October 12, 2017
Evaluation of BRCA1 Large Genomic Rearrangements in Group of Egyptian Female Breast Cancer Patients Using MLPAOla M Eid, Eman A El Ghoroury, Maha M Eid, et al.
Current Pharmaceutical Biotechnology|March 21, 2020
Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic AberrationsHanaa R M Attia, Amany H Abdelrahman, Mona H Ibrahim, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotypeGhada M H Abdel-Salam, Laura Flores-Sarnat, Mona O El-Ruby, et al.
Congenital Anomalies|December 30, 2015
Expanding the mutation and clinical spectrum of Roberts syndromeHanan H Afifi, Ghada M H Abdel-Salam, Maha M Eid, et al.
Cytogenetic and Genome Research|March 19, 2020
Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-InactivationAmal M Mohamed, Maha M Eid, Ola M Eid, et al.
Journal of Pediatric Urology|December 19, 2012
Anti-diuretic hormone and genetic study in primary nocturnal enuresisAmany A A Fatouh, Ayat A Motawie, Amany M Abd Al-Aziz, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndromeNoriko Miyake, Ghada Abdel-Salam, Takanori Yamagata, et al.
Journal, Genetic Engineering & Biotechnology|November 10, 2023
Detection of AZFc gene deletion in a cohort of Egyptian patients with idiopathic male infertilityMaha M Eid, Ola M Eid, Amany H Abdelrahman, et al.
American Journal of Medical Genetics. Part A|October 13, 2011
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorderGhada M H Abdel-Salam, Noriko Miyake, Maha M Eid, et al.
Pageof 4