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Genetic analysis of patients with nonsyndromic and syndromic retinitis pigmentosa in Puerto Rico: a genetic legacy.

• Authors : Vargas, José Gustavo¹ (AUTHOR); Izquierdo, Natalio J.² (AUTHOR) ; Oliver, Armando³ (AUTHOR)

• Source: Ophthalmic Genetics. Aug2022, Vol. 43 Issue 4, p454-461. 8p.

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Bietti’s crystalline dystrophy in Nepalese patients: when genetic analysis supports clinical diagnosis

• Authors : Sanyam Bajimaya; Paul S. Bernstein; Barsha Suwal

Subjects: 0301 basic medicine; medicine.medical_specialty; animal structures

• Source: Ophthalmic Genetics. 40:390-392

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Genetic analysis of patients with nonsyndromic and syndromic retinitis pigmentosa in Puerto Rico: a genetic legacy

• Authors : José Gustavo Vargas; Natalio J. Izquierdo; Armando Oliver

Subjects: Ophthalmology; Cross-Sectional Studies; Pediatrics, Perinatology and Child Health

• Source: Ophthalmic genetics. 43(4)

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Genetic analysis of SOX2 and VSX2 genes in 27 Egyptian families with anophthalmia and microphthalmia.

• Authors : Ammar, Tamer H. A.¹ (AUTHOR); Ismail, Somaia¹ (AUTHOR); Mansour, Ossama Abd Al-Motaal² (AUTHOR)

• Source: Ophthalmic Genetics. Sep/Oct2017, Vol. 38 Issue 5, p498-500. 3p.

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Bietti's crystalline dystrophy in Nepalese patients: when genetic analysis supports clinical diagnosis.

• Authors : Suwal B; Department of Ophthalmology, Hospital for Children, Eye, ENT and Rehabilitation Services , Bhaktapur , Nepal.; Bajimaya S

Subjects: Mutation*; Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/*diagnosis ; Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/*genetics Bietti Crystalline Dystrophy

• Source: Ophthalmic genetics [Ophthalmic Genet] 2019 Aug; Vol. 40 (4), pp. 390-392. Date of Electronic Publication: 2019 Sep 12.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Molecular Genetic Analysis of a Consanguineous South Indian Family with Congenital Glaucoma: Relevance of Genetic Testing and Counseling.

• Authors : Ramprasad, Vedam Lakshmi¹ (AUTHOR); George, Ronnie J.² (AUTHOR); Sripriya, Sarangapani¹ (AUTHOR)

• Source: Ophthalmic Genetics. Mar2007, Vol. 28 Issue 1, p17-24. 8p. 1 Black and White Photograph, 2 Diagrams, 2 Charts, 2 Graphs.

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Posterior Polar Cataract: Genetic Analysis of a Large Family.

• Authors : Finzi, Simone^1,2 (AUTHOR); Li, Yingying¹ (AUTHOR); Mitchell, Thomas N.¹ (AUTHOR)

• Source: Ophthalmic Genetics. Sep2005, Vol. 26 Issue 3, p125-130. 6p. 2 Diagrams, 3 Charts.

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Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma.

• Authors : Markandaya, M.¹; Ramesh, T. K.²; Selvaraju, V.¹

• Source: Ophthalmic Genetics. Mar2004, Vol. 25 Issue 1, p11-23. 13p. 1 Black and White Photograph, 3 Diagrams, 1 Chart.

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Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).

• Authors : Kerrison, John B.; Giorda, Roberto; Lenart, Thomas D.

• Source: Ophthalmic Genetics. Dec2001, Vol. 22 Issue 4, p241. 8p. 2 Diagrams, 1 Chart.

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Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucoma

• Authors : Ravi Prakash; Selvaraju; Arun Kumar

Subjects: Adult; Male; genetic structures

• Source: Ophthalmic genetics. 25(1)

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