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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia

Bohlega, Saeed A ; Shinwari, Jameela M ; Al Sharif, Latifa J ; Khalil, Dania S ; Alkhairallah, Thamer S ; Al Tassan, Nada A

BMC medical genetics, 2011-02, Vol.12 (1), p.27-27, Article 27 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles
Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles
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Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles

Khan, Arif O., MD ; Khalil, Dania S., BSc ; Al Sharif, Latifa J., BSc ; Al-Ghadhfan, Faisal E., MD ; Al Tassan, Nada A., PhD

Ophthalmology (Rochester, Minn.), 2010, Vol.117 (1), p.154-158 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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3
Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus
Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus
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Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus

Khan, Arif O. ; Khalil, Dania S. ; Al-Sharif, Latifa J. ; Al-Tassan, Nada A.

Ophthalmic genetics, 2009-11, Vol.30 (4), p.206-207 [Periódico revisado por pares]

England: Informa UK Ltd

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4
Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3)
Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3)
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Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3)

Khan, Arif O ; Shinwari, Jameela ; Abu Dhaim, Nada ; Khalil, Dania ; Al Sharif, Latifa ; Al Tassan, Nada

Molecular vision, 2011-04, Vol.17, p.971-976 [Periódico revisado por pares]

United States: Molecular Vision

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5
Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome
Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome
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Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome

Khan, Arif O ; Shinwari, Jameela ; Al Sharif, Latifa ; Khalil, Dania ; Al-Gehedan, Saeed ; Tassan, Nada A Al

Molecular vision, 2011, Vol.17, p.1997-2002 [Periódico revisado por pares]

United States: Molecular Vision

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6
Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families
Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families
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Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families

Khan, Arif O ; Shinwari, Jameela ; Omar, Aisha ; Al-Sharif, Latifa ; Khalil, Dania S ; Alanazi, Mohammed ; Al-Amri, Abdullah ; Al Tassan, Nada

Molecular vision, 2011-01, Vol.17, p.218-224 [Periódico revisado por pares]

United States: Molecular Vision

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