Sindrome di Pendred (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrome di Pendred" in Italian language version.

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Pendred V, Deaf-mutism and goitre, in Lancet, vol. 2, n. 3808, 1896, p. 532, DOI:10.1016/S0140-6736(01)74403-0.
Pearce JM, Pendred's syndrome, in Eur. Neurol., vol. 58, n. 3, 2007, pp. 189-90, DOI:10.1159/000104724, PMID 17622729.
Reardon W, Coffey R, Phelps PD, et al., Pendred syndrome--100 years of underascertainment? (PDF), in QJM, vol. 90, n. 7, luglio 1997, pp. 443-7, DOI:10.1093/qjmed/90.7.443, PMID 9302427.
Sheffield VC, Kraiem Z, Beck JC, et al., Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification, in Nat. Genet., vol. 12, n. 4, aprile 1996, pp. 424-6, DOI:10.1038/ng0496-424, PMID 8630498.
Coyle B, Coffey R, Armour JA, et al., Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4, in Nat. Genet., vol. 12, n. 4, aprile 1996, pp. 421-3, DOI:10.1038/ng0496-421, PMID 8630497.
Azaiez H, Yang T, Prasad S, et al., Genotype-phenotype correlations for SLC26A4-related deafness, in Hum. Genet., vol. 122, n. 5, dicembre 2007, pp. 451-7, DOI:10.1007/s00439-007-0415-2, PMID 17690912.

karger.com

content.karger.com

Pearce JM, Pendred's syndrome, in Eur. Neurol., vol. 58, n. 3, 2007, pp. 189-90, DOI:10.1159/000104724, PMID 17622729.

nih.gov

ncbi.nlm.nih.gov

Pearce JM, Pendred's syndrome, in Eur. Neurol., vol. 58, n. 3, 2007, pp. 189-90, DOI:10.1159/000104724, PMID 17622729.
Reardon W, Coffey R, Phelps PD, et al., Pendred syndrome--100 years of underascertainment? (PDF), in QJM, vol. 90, n. 7, luglio 1997, pp. 443-7, DOI:10.1093/qjmed/90.7.443, PMID 9302427.
Sheffield VC, Kraiem Z, Beck JC, et al., Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification, in Nat. Genet., vol. 12, n. 4, aprile 1996, pp. 424-6, DOI:10.1038/ng0496-424, PMID 8630498.
Coyle B, Coffey R, Armour JA, et al., Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4, in Nat. Genet., vol. 12, n. 4, aprile 1996, pp. 421-3, DOI:10.1038/ng0496-421, PMID 8630497.
Azaiez H, Yang T, Prasad S, et al., Genotype-phenotype correlations for SLC26A4-related deafness, in Hum. Genet., vol. 122, n. 5, dicembre 2007, pp. 451-7, DOI:10.1007/s00439-007-0415-2, PMID 17690912.

oadoi.org

Pendred V, Deaf-mutism and goitre, in Lancet, vol. 2, n. 3808, 1896, p. 532, DOI:10.1016/S0140-6736(01)74403-0.
Sheffield VC, Kraiem Z, Beck JC, et al., Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification, in Nat. Genet., vol. 12, n. 4, aprile 1996, pp. 424-6, DOI:10.1038/ng0496-424, PMID 8630498.
Coyle B, Coffey R, Armour JA, et al., Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4, in Nat. Genet., vol. 12, n. 4, aprile 1996, pp. 421-3, DOI:10.1038/ng0496-421, PMID 8630497.
Azaiez H, Yang T, Prasad S, et al., Genotype-phenotype correlations for SLC26A4-related deafness, in Hum. Genet., vol. 122, n. 5, dicembre 2007, pp. 451-7, DOI:10.1007/s00439-007-0415-2, PMID 17690912.

oxfordjournals.org

qjmed.oxfordjournals.org

Reardon W, Coffey R, Phelps PD, et al., Pendred syndrome--100 years of underascertainment? (PDF), in QJM, vol. 90, n. 7, luglio 1997, pp. 443-7, DOI:10.1093/qjmed/90.7.443, PMID 9302427.

web.archive.org

National Institute on Deafness and Other Communication Disorders, Pendred Syndrome, su nidcd.nih.gov, ottobre 2006. URL consultato il 5 maggio 2008 (archiviato dall'url originale il 9 maggio 2008).