| 1991 | - | Familial aggregation of a developmental language disorder - Gopnik,Crago | :: | 20 |
| 1998 | - | Neural basis of an inherited speech and language disorder - Vargha-Khadem | :: | 4 |
| 1990 | - | An extended family with a dominantly inherited speech disorder - Hurst,Baraitser,Auger,Graham,Norell | :: | 3 |
| 2001 | - | Characterization of a new subfamily of winged-helix/forkhead - Shu,Yang,Zhang,Lu,Morrisey | :: | 2 |
| 2000 | - | The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder - Lai | :: | 2 |
| 2001 | - | Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts - Semina,Brownell,Mintz-Hittner,Murray,Jamrich | :: | 1 |
| 2000 | - | Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma - Lehmann | :: | 1 |
| 1995 | - | Genetic basis for speci®c language impairment: evidence from a twin study - Bishop,North,Donlan | :: | 1 |
| 2001 | - | The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ ptosis/epicanthus inversus syndrome - Crisponi | :: | 1 |
| 2000 | - | Fourteen and counting: unraveling trinucleotide repeat diseases - Cummings,Zoghbi | :: | 1 |
| 2000 | - | Mutations in FOXC - Fang | :: | 1 |
| 2001 | - | Disruption of a new forkhead/winged-helix protein, scur®n, results in the fatal lymphoproliferative disorder of the scurfy mouse - Brunkow | :: | 1 |
| 1998 | - | Genetic in¯uence on language delay in two-year-old children - Dale | :: | 1 |
| 1995 | - | Praxic and nonverbal cognitive de®cits in a large family with a genetically transmitted speech and language disorder - Vargha-Khadem,Watkins,Alcock,Fletcher,Passingham | :: | 1 |
| 1996 | - | Five years on the wings of fork head - Kaufmann,KnoEchel | :: | 1 |
| 1998 | - | The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p - Nishimura | :: | 1 |
| 2001 | - | X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy - Wildin | :: | 1 |
| 1993 | - | Co-crystal structure of the HNF-3/fork head DNA- recognition motif resembles histone H - Clark,Halay,Lai,Burley | :: | 1 |
| 1998 | - | Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia - Clifton-Bligh | :: | 1 |
| 1993 | - | DNA-binding properties and secondary structural model of the hepatocyte nuclear factor 3/fork head domain - Li,Tucker | :: | 1 |
| 1998 | - | Heritability of poor language achievement among twins - Tomblin,Buckwalter | :: | 1 |
| 2001 | - | A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye - Nishimura | :: | 1 |
| 2000 | - | Haploinsuf®ciency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development - Smith | :: | 1 |
| 1998 | - | A mouse model for hereditary thyroid dysgenesis and cleft palate - De Felice | :: | 1 |
| 1998 | - | Localization of a gene implicated in a severe speech and language disorder - Fisher,Vargha-Khadem,Watkins,Monaco,Pembrey | :: | 1 |
| 1998 | - | Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld- Rieger anomaly - Mears | :: | 1 |
| 2000 | - | Uni®ed nomenclature for the winged helix/forkhead transcription factors - Kaestner,KnoEchel,Martinez | :: | 1 |