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January 2014 - Volume 3 - Issue 1 - Contributor Index

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Abdel-Hamid, Mohamed

A report of another Egyptian patient with Temtamy preaxial brachydactyly syndrome associated with a novel nonsense CHSY1 mutation

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Aglan, Mona

A report of another Egyptian patient with Temtamy preaxial brachydactyly syndrome associated with a novel nonsense CHSY1 mutation

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Al Suliman, Ibrahim S.

Familial adenomatous polyposis: two different APC gene mutations in two unrelated Arab families with differing response to genetic counselling

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Al-Elwani, Farah L.

Familial adenomatous polyposis: two different APC gene mutations in two unrelated Arab families with differing response to genetic counselling

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Eid, Maha M.

Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients

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El-bassyouni, Hala T.

Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss

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Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients

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El-Kamah, Ghada Y.

Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients

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Elbagoury, Nagham M.

Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss

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Elruby, Mona O.

Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss

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Essawi, Mona L.

Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss

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Fateen, Ekram M.

Biochemical diagnosis of mucopolysaccharidoses over 11 years: the Egyptian experience

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Ghorab, Eman A.

Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss

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Gouda, Amr S.

Biochemical diagnosis of mucopolysaccharidoses over 11 years: the Egyptian experience

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Hamamy, Hanan

Epidemiological profile of neural tube defects in Arab countries

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Ibrahim, Mona M.

Biochemical diagnosis of mucopolysaccharidoses over 11 years: the Egyptian experience

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Ismail, Somaia

A report of another Egyptian patient with Temtamy preaxial brachydactyly syndrome associated with a novel nonsense CHSY1 mutation

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Marafie, Makia J.

Familial adenomatous polyposis: two different APC gene mutations in two unrelated Arab families with differing response to genetic counselling

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Mohammed, Ola S.

Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss

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Mosaad, Rehab M.

Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients

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