Works matching IS 20908571 AND DT 2017 AND VI 6 AND IP 2
Results: 5
Nager acrofacial dysostosis with a novel mutation in SF3B4 and developmental retardation in an Egyptian child.
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- Middle East Journal of Medical Genetics, 2017, v. 6, n. 2, p. 82, doi. 10.1097/01.MXE.0000521018.95032.31
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- Article
Biochemical study of glycogen storage disease type II (Pompe disease) in Egyptian infants.
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- Middle East Journal of Medical Genetics, 2017, v. 6, n. 2, p. 75, doi. 10.1097/01.MXE.0000521019.02657.75
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- Article
Diagnostic approach of floppy infants: a study in Fayoum University Hospital, Egypt.
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- Middle East Journal of Medical Genetics, 2017, v. 6, n. 2, p. 70, doi. 10.1097/01.MXE.0000520658.04653.ea
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- Article
Mutational analysis of a cohort of Egyptian patients with Gaucher disease.
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- Middle East Journal of Medical Genetics, 2017, v. 6, n. 2, p. 61, doi. 10.1097/01.MXE.0000520527.54080.ab
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- Article
The scope of orodental genetics.
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- Middle East Journal of Medical Genetics, 2017, v. 6, n. 2, p. 49, doi. 10.1097/01.MXE.0000521017.17904.8f
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- Article