Salamanca-Gómez F

Language: Spanish
References: 10
Page: 103-104
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REFERENCES

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2. Dale PS, et al. Genetic influence on language delay in two-years-old children. Nature Neurosci. 1998;1:324-328.

3. Hurst JA, Baraitsser M, Auger E, Graham F y Norell S. An extended family with a dominantly inherited speech disorder. Dev. Med. Child Neurol. 1990;32:347-355.

4. Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP y Pembrey ME. Localization of a gene implicated in a severe speech and language disorder. Nature Genet. 1998;18:168-170.

5. Lai CSL et al. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. Am. J. Hum Genet. 2000;67:357-368.

6. Lai CSL, Ficher SE, Hurst JA, Vargha-Khadem F y Monaco AP. A Forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001;413 :519-523.

7. Nishimura DY et al. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nature Genet. 1998;19:140147.

8. Clifton-Bling RJ, et al. Mutation of the gene encoding human TTF2 associated with thyroid agenesis, cleft palate and choanal atresia. Nature Genet. 1998;19:399-401.

9. Fang J et al. Mutation in FOXC2(MFH1) a forkhead family transcription factor are responsible for the hereditary lymphedema-distichiasis syndrome. Am J. Hum Genet. 2000;67:1382-1388.

10. Crispone F, et al. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ ptosis/ epicanthus inversus syndrome. Nature Genet. 2001;27:159-166.