PubMed (cited) for id: 274600

Year	Number of Results
1950	1
1957	1
1958	2
1960	1
1962	1
1964	1
1965	1
1967	2
1968	1
1969	1
1970	1
1972	1
1973	2
1974	2
1975	1
1986	1
1996	3
1997	4
1998	2
1999	2
2000	3
2001	3
2002	1
2003	2
2005	2
2007	1
2010	1
2024	0

1

Spectrum and frequency of SLC26A4 mutations among Czech patients with early hearing loss with and without Enlarged Vestibular Aqueduct (EVA).

Pourová R, Janousek P, Jurovcík M, Dvoráková M, Malíková M, Rasková D, Bendová O, Leonardi E, Murgia A, Kabelka Z, Astl J, Seeman P. Pourová R, et al. Ann Hum Genet. 2010 Jul;74(4):299-307. doi: 10.1111/j.1469-1809.2010.00581.x. Ann Hum Genet. 2010. PMID: 20597900

2

Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4).

Yang T, Vidarsson H, Rodrigo-Blomqvist S, Rosengren SS, Enerback S, Smith RJ. Yang T, et al. Am J Hum Genet. 2007 Jun;80(6):1055-63. doi: 10.1086/518314. Epub 2007 Apr 23. Am J Hum Genet. 2007. PMID: 17503324 Free PMC article.

3

Genetics of congenital hypothyroidism.

Park SM, Chatterjee VK. Park SM, et al. J Med Genet. 2005 May;42(5):379-89. doi: 10.1136/jmg.2004.024158. J Med Genet. 2005. PMID: 15863666 Free PMC article. Review.

4

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.

Pryor SP, Madeo AC, Reynolds JC, Sarlis NJ, Arnos KS, Nance WE, Yang Y, Zalewski CK, Brewer CC, Butman JA, Griffith AJ. Pryor SP, et al. J Med Genet. 2005 Feb;42(2):159-65. doi: 10.1136/jmg.2004.024208. J Med Genet. 2005. PMID: 15689455 Free PMC article. No abstract available.

5

A study of a family of goitrous cretins.

STANBURY JB, HEDGE AN. STANBURY JB, et al. J Clin Endocrinol Metab. 1950 Nov;10(11):1471-84. doi: 10.1210/jcem-10-11-1471. J Clin Endocrinol Metab. 1950. PMID: 14794763 No abstract available.

6

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.

Tsukamoto K, Suzuki H, Harada D, Namba A, Abe S, Usami S. Tsukamoto K, et al. Eur J Hum Genet. 2003 Dec;11(12):916-22. doi: 10.1038/sj.ejhg.5201073. Eur J Hum Genet. 2003. PMID: 14508505

7

ASSOCIATION OF CONGENITAL DEAFNESS WITH GOITRE (PENDRED'S SYNDROME) A STUDY OF 207 FAMILIES.

FRASER GR. FRASER GR. Ann Hum Genet. 1965 Mar;28:201-49. doi: 10.1111/j.1469-1809.1964.tb00479.x. Ann Hum Genet. 1965. PMID: 14304636 No abstract available.

8

CONGENITAL DEAFNESS AND GOITER. STUDIES OF A PATIENT WITH A COCHLEAR DEFECT AND INADEQUATE FORMATION OF IODOTHYRONINES.

HOLLANDER CS, PROUT TE, RIENHOFF M, RUBEN RJ, ASPER SP Jr. HOLLANDER CS, et al. Am J Med. 1964 Oct;37:630-7. doi: 10.1016/0002-9343(64)90075-0. Am J Med. 1964. PMID: 14215850 No abstract available.

9

Deafness with sporadic goiter. Pendred's syndrome.

BATSAKIS JG, NISHIYAMA RH. BATSAKIS JG, et al. Arch Otolaryngol. 1962 Nov;76:401-6. doi: 10.1001/archotol.1962.00740050413004. Arch Otolaryngol. 1962. PMID: 13966825 No abstract available.

10

The syndrome of sporadic goitre and congenital deafness.

FRASER GR, MORGANS ME, TROTTER WR. FRASER GR, et al. Q J Med. 1960 Apr;29:279-95. Q J Med. 1960. PMID: 13824627 No abstract available.

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