Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment

A forkhead-domain gene is mutated in a severe speech and language disorder

Cecilia Lai, Simon E. Fisher, Jane A. Hurst et al. · Nature · 2001 · 2.1K citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Laura Crisponi, Manila Deiana, Angela Loi et al. · Nature Genetics · 2001 · 977 citations

Life Sciences, Genetics, Molecular Genetics +5

Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Jianming Fang, Susan L. Dagenais, Robert P. Erickson et al. · The American Journal of Human Genetics · 2000 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Localisation of a gene implicated in a severe speech and language disorder

Simon E. Fisher, Faraneh Vargha‐Khadem, Kate E. Watkins et al. · Nature Genetics · 1998 · 486 citations · Full text

Life Sciences, Genetics, Speech-language Pathology +15

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

Darryl Nishimura, Ruth E. Swiderski, Wallace L.M. Alward et al. · Nature Genetics · 1998 · 472 citations

Life Sciences, Genetics, Molecular Genetics +10