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Mennat I. Mehrez

16

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79

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Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience

2021
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Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations

2021 Genes
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Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.

2020 American Journal of Human Genetics
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Lenz–Majewski syndrome in a patient from Egypt

2019 American Journal of Medical Genetics Part A
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AB0003 A galnt3 gene mutation in two sibs with chronic recurrent multifocal osteomyelitis associated with hyperphosphatemic familial tumoral calcinosis

2018 Annals of the Rheumatic Diseases
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Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect

2018 Osteoporosis International
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Lipoid proteinosis: A clinical and molecular study in Egyptian patients

2017 Gene
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Expanding the mutation and clinical spectrum of Roberts syndrome

2016 Congenital Anomalies
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Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations

2015 American Journal of Medical Genetics Part A
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Hutchinson-Gilford progeria versus mandibuloacral dysplasia

2014 Indian Journal of Dermatology
- Mennat I. Mehrez
- Mostafa Ibrahim Mostafa
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