Double Jeopardy: Blepharophimosis Syndrome with Congenital Nasolacrimal Duct Obstruction in Twins

By Mukherjee Bipasha   Shahid Alam Md.  

Orbit, Vol. 32, Iss. 5, 2013-10 ,pp. : 318-320

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A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: Differential role of the polyalanine tract in the development of the ovary and the eyelid

By Kosaki Kenjiro   Ogata Tsutomu   Kosaki Rika   Sato Seiji   Matsuo Nobutake  

Ophthalmic Genetics, Vol. 23, Iss. 1, 2002-03 ,pp. : 43-47

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The Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome (BPES)

By Tyers Anthony G.  

Orbit, Vol. 30, Iss. 5, 2011-10 ,pp. : 199-201

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Familial Blepharophimosis-Like Syndrome with Esotropia, Uveal Coloboma, and Short Stature

By Khan Arif   Alam Syed   Aldahmesh Mohammed   Rajab Mohammed   Meyer Brian  

Ophthalmic Genetics, Vol. 27, Iss. 3, 2006-09 ,pp. : 79-82

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Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma

By Finzi Simone   Pinto Carla F.   Wiggs Janey L.  

Ophthalmic Genetics, Vol. 22, Iss. 1, 2001-03 ,pp. : 35-41

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