FOXL2 mutations in Indian families with blepharophimosis-ptosis-epicanthus inversus syndrome. | J Genet; 2007 Aug; 86(2): 165-8 | IMSEAR

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FOXL2 mutations in Indian families with blepharophimosis-ptosis-epicanthus inversus syndrome.

Nallathambi, Jeyabalan; Neethirajan, Guruswamy; Usha, Kim; Jitendra, Jethani; De Baere, Elfride; Sundaresan, Periasamy.

J Genet ; 2007 Aug; 86(2): 165-8

Article in En | IMSEAR | ID: sea-114244

Subject(s)

Blepharophimosis/complications; Child, Preschool; DNA Mutational Analysis; Eye Diseases/congenital; Family; Female; Forkhead Transcription Factors/genetics; Humans; India; Infant; Male; Mutation; Pedigree; Syndrome

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Full text: 1 Index: IMSEAR Main subject: Pedigree / Syndrome / Female / Humans / Male / DNA Mutational Analysis / Family / Child, Preschool / Blepharophimosis / Forkhead Transcription Factors Country/Region as subject: Asia Language: En Journal: J Genet Year: 2007 Type: Article

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Full text: 1 Index: IMSEAR Main subject: Pedigree / Syndrome / Female / Humans / Male / DNA Mutational Analysis / Family / Child, Preschool / Blepharophimosis / Forkhead Transcription Factors Country/Region as subject: Asia Language: En Journal: J Genet Year: 2007 Type: Article