Van Camp G - Search Results

1

Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea.

Van Laer L, Van Camp G, van Zuijlen D, Green ED, Verstreken M, Schatteman I, Van de Heyning P, Balemans W, Coucke P, Greinwald JH, Smith RJ, Huizing E, Willems P. Van Laer L, et al. Among authors: van de heyning p, van camp g, van zuijlen d. Eur J Hum Genet. 1997 Nov-Dec;5(6):397-405. Eur J Hum Genet. 1997. PMID: 9450185

2

Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.

Van Camp G, Backhovens H, Cruts M, Wehnert A, Van Hul W, Stinissen P, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c, van hul w. Hum Genet. 1991 Oct;87(6):649-53. doi: 10.1007/BF00201718. Hum Genet. 1991. PMID: 1682232

3

An informative MspI polymorphism detected at the D21S16 locus.

Van Camp G, Vandenberghe A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c. Hum Genet. 1990 Jun;85(1):140. doi: 10.1007/BF00276344. Hum Genet. 1990. PMID: 1694162 No abstract available.

4

Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids.

Van Camp G, Van Hul W, Backhovens H, Stinissen P, Wehnert A, Patterson D, Vandenberghe A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c, van hul w. Somat Cell Mol Genet. 1990 May;16(3):241-9. doi: 10.1007/BF01233360. Somat Cell Mol Genet. 1990. PMID: 1972817

5

Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniques.

Van Hul W, Backhovens H, Van Camp G, Stinissen P, Cruts M, Wehnert A, Van Broeckhoven C. Van Hul W, et al. Among authors: van broeckhoven c, van camp g. Hum Genet. 1991 Jun;87(2):109-11. doi: 10.1007/BF00204162. Hum Genet. 1991. PMID: 2066096

6

Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome.

Van Camp G, Stinissen P, Van Hul W, Backhovens H, Wehnert A, Vandenberge A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c, van hul w. Hum Genet. 1989 Aug;83(1):58-60. doi: 10.1007/BF00274149. Hum Genet. 1989. PMID: 2570018

7

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Van Camp G, Van Thienen MN, Handig I, Van Roy B, Rao VS, Milunsky A, Read AP, Baldwin CT, Farrer LA, Bonduelle M, et al. Van Camp G, et al. Among authors: van thienen mn, van roy b. J Med Genet. 1995 Jul;32(7):531-6. doi: 10.1136/jmg.32.7.531. J Med Genet. 1995. PMID: 7562965 Free PMC article.

8

X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene.

Fransen E, Schrander-Stumpel C, Vits L, Coucke P, Van Camp G, Willems PJ. Fransen E, et al. Among authors: van camp g. Hum Mol Genet. 1994 Dec;3(12):2255-6. doi: 10.1093/hmg/3.12.2255. Hum Mol Genet. 1994. PMID: 7881431 No abstract available.

9

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

Vits L, Van Camp G, Coucke P, Fransen E, De Boulle K, Reyniers E, Korn B, Poustka A, Wilson G, Schrander-Stumpel C, et al. Vits L, et al. Among authors: van camp g. Nat Genet. 1994 Jul;7(3):408-13. doi: 10.1038/ng0794-408. Nat Genet. 1994. PMID: 7920660

10

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.

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