Van Camp G - Search Results

1

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.

Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Van Camp G, Berlin CI, Oddoux C, Ostrer H, Keats B, Friedman TB. Morell RJ, et al. Among authors: van camp g. N Engl J Med. 1998 Nov 19;339(21):1500-5. doi: 10.1056/NEJM199811193392103. N Engl J Med. 1998. PMID: 9819448 Free article.

2

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.

Coucke P, Van Camp G, Djoyodiharjo B, Smith SD, Frants RR, Padberg GW, Darby JK, Huizing EH, Cremers CW, Kimberling WJ, et al. Coucke P, et al. Among authors: van camp g. N Engl J Med. 1994 Aug 18;331(7):425-31. doi: 10.1056/NEJM199408183310702. N Engl J Med. 1994. PMID: 8035838 Free article.

3

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

Lench NJ, Markham AF, Mueller RF, Kelsell DP, Smith RJ, Willems PJ, Schatteman I, Capon H, Van De Heyning PJ, Van Camp G. Lench NJ, et al. Among authors: van de heyning pj, van camp g. J Med Genet. 1998 Feb;35(2):151-2. doi: 10.1136/jmg.35.2.151. J Med Genet. 1998. PMID: 9507396 Free PMC article.

4

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method.

Storm K, Willocx S, Flothmann K, Van Camp G. Storm K, et al. Among authors: van camp g. Hum Mutat. 1999;14(3):263-6. doi: 10.1002/(SICI)1098-1004(1999)14:3<263::AID-HUMU10>3.0.CO;2-X. Hum Mutat. 1999. PMID: 10477435

5

Autosomal recessive nonsyndromic hearing loss.

Sundstrom RA, Van Laer L, Van Camp G, Smith RJ. Sundstrom RA, et al. Among authors: van laer l, van camp g. Am J Med Genet. 1999 Sep 24;89(3):123-9. doi: 10.1002/(sici)1096-8628(19990924)89:3<123::aid-ajmg2>3.0.co;2-p. Am J Med Genet. 1999. PMID: 10704186 Review.

6

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

Van Laer L, Coucke P, Mueller RF, Caethoven G, Flothmann K, Prasad SD, Chamberlin GP, Houseman M, Taylor GR, Van de Heyning CM, Fransen E, Rowland J, Cucci RA, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: van de heyning cm, van camp g. J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515. J Med Genet. 2001. PMID: 11483639 Free PMC article.

7

Deafness genes and their diagnostic applications.

Cryns K, Van Camp G. Cryns K, et al. Among authors: van camp g. Audiol Neurootol. 2004 Jan-Feb;9(1):2-22. doi: 10.1159/000074183. Audiol Neurootol. 2004. PMID: 14676470 Review.

8

A genotype-phenotype correlation for GJB2 (connexin 26) deafness.

Cryns K, Orzan E, Murgia A, Huygen PL, Moreno F, del Castillo I, Chamberlin GP, Azaiez H, Prasad S, Cucci RA, Leonardi E, Snoeckx RL, Govaerts PJ, Van de Heyning PH, Van de Heyning CM, Smith RJ, Van Camp G. Cryns K, et al. Among authors: van de heyning ph, van de heyning cm, van camp g. J Med Genet. 2004 Mar;41(3):147-54. doi: 10.1136/jmg.2003.013896. J Med Genet. 2004. PMID: 14985372 Free PMC article.

9

GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population.

Snoeckx RL, Djelantik B, Van Laer L, Van de Heyning P, Van Camp G. Snoeckx RL, et al. Among authors: van laer l, van de heyning p, van camp g. Am J Med Genet A. 2005 Jun 1;135(2):126-9. doi: 10.1002/ajmg.a.30726. Am J Med Genet A. 2005. PMID: 15832357

10

Mutation analysis of the GJB2 (connexin 26) gene in Egypt.

Snoeckx RL, Hassan DM, Kamal NM, Van Den Bogaert K, Van Camp G. Snoeckx RL, et al. Among authors: van den bogaert k, van camp g. Hum Mutat. 2005 Jul;26(1):60-1. doi: 10.1002/humu.9350. Hum Mutat. 2005. PMID: 15954104

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