Wauters J - Search Results

1

Identification and characterization of a novel member of the EXT gene family, EXTL2.

Wuyts W, Van Hul W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Van Agtmael T, Bossuyt P, Willems PJ. Wuyts W, et al. Among authors: wauters j. Eur J Hum Genet. 1997 Nov-Dec;5(6):382-9. Eur J Hum Genet. 1997. PMID: 9450183

2

Positional cloning of a gene involved in hereditary multiple exostoses.

Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ. Wuyts W, et al. Among authors: wauters j. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688

3

Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family.

Van Hul W, Wuyts W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Bossuyt P, Willems PJ. Van Hul W, et al. Among authors: wauters j. Genomics. 1998 Jan 15;47(2):230-7. doi: 10.1006/geno.1997.5101. Genomics. 1998. PMID: 9479495

4

Molecular and clinical examination of an Italian DEFECT11 family.

Wuyts W, Di Gennaro G, Bianco F, Wauters J, Morocutti C, Pierelli F, Bossuyt P, Van Hul W, Casali C. Wuyts W, et al. Among authors: wauters j. Eur J Hum Genet. 1999 Jul;7(5):579-84. doi: 10.1038/sj.ejhg.5200339. Eur J Hum Genet. 1999. PMID: 10439965

5

Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.

Wuyts W, Roland D, Lüdecke HJ, Wauters J, Foulon M, Van Hul W, Van Maldergem L. Wuyts W, et al. Among authors: wauters j. Am J Med Genet. 2002 Dec 15;113(4):326-32. doi: 10.1002/ajmg.10845. Am J Med Genet. 2002. PMID: 12457403

6

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: wauters j. Hum Mol Genet. 1993 May;2(5):583-9. doi: 10.1093/hmg/2.5.583. Hum Mol Genet. 1993. PMID: 8518797

7

Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mapping.

Van Hul W, Hong G, Wauters J, Van Hul E, Nowak N, Shows TB, Willems PJ, Merregaert J. Van Hul W, et al. Among authors: wauters j. Cytogenet Cell Genet. 1996;74(3):218-9. doi: 10.1159/000134417. Cytogenet Cell Genet. 1996. PMID: 8941377 No abstract available.

8

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.

Van Camp G, Kunst H, Flothmann K, McGuirt W, Wauters J, Marres H, Verstreken M, Bespalova IN, Burmeister M, Van de Heyning PH, Smith RJ, Willems PJ, Cremers CW, Lesperance MM. Van Camp G, et al. Among authors: wauters j. J Med Genet. 1999 Jul;36(7):532-6. J Med Genet. 1999. PMID: 10424813 Free PMC article.

9

Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).

Holinski-Feder E, Reyniers E, Uhrig S, Golla A, Wauters J, Kroisel P, Bossuyt P, Rost I, Jedele K, Zierler H, Schwab S, Wildenauer D, Speicher MR, Willems PJ, Meitinger T, Kooy RF. Holinski-Feder E, et al. Among authors: wauters j. Am J Hum Genet. 2000 Jan;66(1):16-25. doi: 10.1086/302703. Am J Hum Genet. 2000. PMID: 10631133 Free PMC article.

10

Regional mapping of a liver alpha-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp.

Wauters JG, Bossuyt PJ, Davidson J, Hendrickx J, Kilimann MW, Willems PJ. Wauters JG, et al. Cytogenet Cell Genet. 1992;60(3-4):194-6. doi: 10.1159/000133334. Cytogenet Cell Genet. 1992. PMID: 1505214

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