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January 2015 - Volume 4 - Issue 1 - Contributor Index

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Abdel-Hamid, Mohamed

Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

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Abdel-Hamid, Mohamed S.

Mutational spectrum of COL1A1 and COL1A2 in Egyptian patients with autosomal dominant osteogenesis imperfecta with clinical severity score and genotype/phenotype correlation

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Abdel-Messih, Ibrahim Y.

Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia

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Abualhasan, Sawsan J.

A rare case of isochromosome 10: i(10p) and i(10q)

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Addissie, Yonit A.

Muenke syndrome

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Aglan, Mona S.

Mutational spectrum of COL1A1 and COL1A2 in Egyptian patients with autosomal dominant osteogenesis imperfecta with clinical severity score and genotype/phenotype correlation

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Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

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Al-Hathal, Muneef

A case report of FATCO syndrome: fibular aplasia, tibial campomelia, and oligosyndactyly

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Alrohaif, Hadil E.

A case report of FATCO syndrome: fibular aplasia, tibial campomelia, and oligosyndactyly

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Antonarakis, Stylianos E.

Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

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Bastaki, Laila A.

A case report of FATCO syndrome: fibular aplasia, tibial campomelia, and oligosyndactyly

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Effat, Laila K.

Mutational spectrum of COL1A1 and COL1A2 in Egyptian patients with autosomal dominant osteogenesis imperfecta with clinical severity score and genotype/phenotype correlation

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Eid, Maha M.

Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia

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El-Azhary, Nermeen H.

Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia

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El-Kamah, Ghada Y.

Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia

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Elbastawisy, Hanan I.

A rare case of isochromosome 10: i(10p) and i(10q)

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Ghaly, Samuel W.

A rare case of isochromosome 10: i(10p) and i(10q)

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Hamamy, Hanan

Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

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Ismail, Somaia

Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

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Ismail, Somaia M.

Mutational spectrum of COL1A1 and COL1A2 in Egyptian patients with autosomal dominant osteogenesis imperfecta with clinical severity score and genotype/phenotype correlation

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