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Asmaa K Amin

Showing results (1-10 of 8) with videos related to

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Molecular Cytogenetics|March 15, 2024
11p13 microduplication: a differential diagnosis of Silver-Russell syndrome?Asmaa K Amin, Jeremias Krause, Thomas Eggermann
Molecular Syndromology|January 2, 2023
Mosaic Variegated Aneuploidy Syndrome and Noonan Syndrome in the Same FamilyChristian T Hübner, Asmaa K Amin, Daniela Dey, et al.
Journal of Prosthodontics : Official Journal of the American College of Prosthodontists|March 5, 2019
A Genetic Association Study of a Specific Gene and Severe Form of Resorption in the Edentulous Mandible in the Egyptian PopulationSamar M Emam, Asmaa K Amin, Noha M Issa, et al.
Clinical Genetics|October 15, 2025
Genetic and Clinical Spectrum of Osteogenesis Imperfecta in an Egyptian Cohort With a High Rate of Lethal PhenotypesGhada Elhady, Asmaa K Amin, Asier Iturrate, et al.
Clinical Genetics|December 12, 2024
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot StudyLuise Kessler, Jeremias Krause, Florian Kraft, et al.
Bone|November 19, 2018
Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypesEliza Thompson, Ebtesam Abdalla, Andrea Superti-Furga, et al.
Clinical Genetics|April 30, 2025
Analysis of Copy Number Variants Is an Important Consideration in Exome SequencingAsmaa K Amin, Sara H El-Dessouky, Marwa Abd Elmaksoud, et al.
Journal of Medical Genetics|March 26, 2024
Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosisUmut Altunoglu, Adrian Palencia-Campos, Nilay Güneş, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular Cytogenetics|March 15, 2024
11p13 microduplication: a differential diagnosis of Silver-Russell syndrome?Asmaa K Amin, Jeremias Krause, Thomas Eggermann
Molecular Syndromology|January 2, 2023
Mosaic Variegated Aneuploidy Syndrome and Noonan Syndrome in the Same FamilyChristian T Hübner, Asmaa K Amin, Daniela Dey, et al.
Journal of Prosthodontics : Official Journal of the American College of Prosthodontists|March 5, 2019
A Genetic Association Study of a Specific Gene and Severe Form of Resorption in the Edentulous Mandible in the Egyptian PopulationSamar M Emam, Asmaa K Amin, Noha M Issa, et al.
Clinical Genetics|October 15, 2025
Genetic and Clinical Spectrum of Osteogenesis Imperfecta in an Egyptian Cohort With a High Rate of Lethal PhenotypesGhada Elhady, Asmaa K Amin, Asier Iturrate, et al.
Clinical Genetics|December 12, 2024
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot StudyLuise Kessler, Jeremias Krause, Florian Kraft, et al.
Bone|November 19, 2018
Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypesEliza Thompson, Ebtesam Abdalla, Andrea Superti-Furga, et al.
Clinical Genetics|April 30, 2025
Analysis of Copy Number Variants Is an Important Consideration in Exome SequencingAsmaa K Amin, Sara H El-Dessouky, Marwa Abd Elmaksoud, et al.
Journal of Medical Genetics|March 26, 2024
Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosisUmut Altunoglu, Adrian Palencia-Campos, Nilay Güneş, et al.
Pageof 1