Coucke P - Search Results

1

Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Willems PJ, Vits L, Raeymaekers P, Beuten J, Coucke P, Holden JJ, Van Broeckhoven C, Warren ST, Sagi M, Robinson D, et al. Willems PJ, et al. Among authors: coucke p. Am J Hum Genet. 1992 Aug;51(2):307-15. Am J Hum Genet. 1992. PMID: 1642232 Free PMC article.

2

Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22.

Willems PJ, Hendrickx J, Van der Auwera BJ, Vits L, Raeymaekers P, Coucke PJ, Van den Bergh I, Berger R, Smit GP, Van Broeckhoven C, et al. Willems PJ, et al. Among authors: coucke pj. Genomics. 1991 Apr;9(4):565-9. doi: 10.1016/0888-7543(91)90347-h. Genomics. 1991. PMID: 1674721

3

Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family.

Willems PJ, Vits L, Wanders RJ, Coucke PJ, Van der Auwera BJ, Van Elsen AF, Raeymaekers P, Van Broeckhoven C, Schutgens RB, Dacremont G, et al. Willems PJ, et al. Among authors: coucke pj. Arch Neurol. 1990 Jun;47(6):665-9. doi: 10.1001/archneur.1990.00530060077022. Arch Neurol. 1990. PMID: 2161209

4

Two brothers with mental retardation discordant for the fragile-X syndrome.

Van Roy BC, Willems PJ, Vits LJ, Ceulemans BP, Coucke PJ, Van der Auwera BJ, Lormans JA, Dumon JE. Van Roy BC, et al. Among authors: coucke pj. Am J Med Genet. 1990 May;36(1):122-5. doi: 10.1002/ajmg.1320360124. Am J Med Genet. 1990. PMID: 2333901

5

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.

Willems PJ, Dijkstra I, Van der Auwera BJ, Vits L, Coucke P, Raeymaekers P, Van Broeckhoven C, Consalez GG, Freeman SB, Warren ST, et al. Willems PJ, et al. Among authors: coucke p. Genomics. 1990 Oct;8(2):367-70. doi: 10.1016/0888-7543(90)90294-5. Genomics. 1990. PMID: 1979056

6

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: coucke p. 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.

7

Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family.

Coucke P, Vits L, Van Camp G, Serville F, Lyonnet S, Kenwrick S, Rosenthal A, Wehnert M, Munnich A, Willems PJ. Coucke P, et al. Hum Mol Genet. 1994 Apr;3(4):671-3. doi: 10.1093/hmg/3.4.671. Hum Mol Genet. 1994. PMID: 8069317 No abstract available.

8

Molecular study of chromosome 15 in 22 patients with Angelman syndrome.

Beuten J, Mangelschots K, Buntinx I, Coucke P, Brouwer OF, Hennekam RC, Van Broeckhoven C, Willems PJ. Beuten J, et al. Among authors: coucke p. Hum Genet. 1993 Jan;90(5):489-95. doi: 10.1007/BF00217446. Hum Genet. 1993. PMID: 8094063

9

A duplication in the L1CAM gene associated with X-linked hydrocephalus.

Van Camp G, Vits L, Coucke P, Lyonnet S, Schrander-Stumpel C, Darby J, Holden J, Munnich A, Willems PJ. Van Camp G, et al. Among authors: coucke p. Nat Genet. 1993 Aug;4(4):421-5. doi: 10.1038/ng0893-421. Nat Genet. 1993. PMID: 8401593

10

X-linked liver glycogenosis: localization and isolation of a candidate gene.

Hendrickx J, Coucke P, Bossuyt P, Wauters J, Raeymaekers P, Marchau F, Smit GP, Stolte I, Sardharwalla IB, Berthelot J, et al. Hendrickx J, et al. Among authors: coucke p. Hum Mol Genet. 1993 May;2(5):583-9. doi: 10.1093/hmg/2.5.583. Hum Mol Genet. 1993. PMID: 8518797

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

536 results

Search Page

Filters