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Results: 6

1.

A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.

Van Camp G, Coucke PJ, Akita J, Fransen E, Abe S, De Leenheer EM, Huygen PL, Cremers CW, Usami S.

Hum Mutat. 2002 Jul;20(1):15-9.

PMID:
12112653
[PubMed - indexed for MEDLINE]
2.

KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.

Nie L.

Curr Opin Otolaryngol Head Neck Surg. 2008 Oct;16(5):441-4. doi: 10.1097/MOO.0b013e32830f4aa3. Review.

PMID:
18797286
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing.

Finsterer J, Fellinger J.

Int J Pediatr Otorhinolaryngol. 2005 May;69(5):621-47. Review.

PMID:
15850684
[PubMed - indexed for MEDLINE]
4.

Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.

Chen AH, Mueller RF, Prasad SD, Greinwald JH Jr, Manaligod J, Muilenburg AC, Verhoeven K, Van Camp G, Smith RJ.

Arch Otolaryngol Head Neck Surg. 1998 Jan;124(1):20-4. Review.

PMID:
9440775
[PubMed - indexed for MEDLINE]
5.

New potassium channel gene families in flies and mammals: from mutants to molecules.

Ganetzky B, Warmke JW, Robertson G, Pallanck L.

Soc Gen Physiol Ser. 1995;50:29-39. Review. No abstract available.

PMID:
7676322
[PubMed - indexed for MEDLINE]
6.

Two further British families with the 'cryohydrocytosis' form of hereditary stomatocytosis.

Haines PG, Jarvis HG, King S, Noormohamed FH, Chetty MC, Fisher J, Hill P, Nicolaou A, Stewart GW.

Br J Haematol. 2001 Jun;113(4):932-7. Review.

PMID:
11442486
[PubMed - indexed for MEDLINE]

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