Works matching IS 20908571 AND DT 2014 AND VI 3 AND IP 1
Results: 6
A report of another Egyptian patient with Temtamy preaxial brachydactyly syndrome associated with a novel nonsense CHSY1 mutation.
- Published in:
- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 37, doi. 10.1097/01.MXE.0000438177.01557.f0
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- Article
Familial adenomatous polyposis.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 31, doi. 10.1097/01.MXE.0000441099.60123.9c
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- Article
Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 24, doi. 10.1097/01.MXE.0000438179.47299.3c
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- Article
Biochemical diagnosis of mucopolysaccharidoses over 11 years.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 16, doi. 10.1097/01.MXE.0000438178.09181.43
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- Article
Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 11, doi. 10.1097/01.MXE.0000438176.01557.b9
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- Article
Epidemiological profile of neural tube defects in Arab countries.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 1, doi. 10.1097/01.MXE.0000438175.24428.e1
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- Article