Bossuyt P - Search Results

1

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: bossuyt p. Am J Hum Genet. 2000 Jan;66(1):16-25. doi: 10.1086/302703. Am J Hum Genet. 2000. PMID: 10631133 Free PMC article.

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: bossuyt p. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688

3

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: bossuyt p. Eur J Hum Genet. 1997 Nov-Dec;5(6):382-9. Eur J Hum Genet. 1997. PMID: 9450183

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: bossuyt p. Eur J Hum Genet. 1999 Jul;7(5):579-84. doi: 10.1038/sj.ejhg.5200339. Eur J Hum Genet. 1999. PMID: 10439965

5

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. Among authors: bossuyt pj. Cytogenet Cell Genet. 1992;60(3-4):194-6. doi: 10.1159/000133334. Cytogenet Cell Genet. 1992. PMID: 1505214

6

Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion.

Wauters JG, Bossuyt PJ, Roelen L, van Roy B, Dumon J. Wauters JG, et al. Among authors: bossuyt pj. Clin Genet. 1993 Nov;44(5):262-9. doi: 10.1111/j.1399-0004.1993.tb03894.x. Clin Genet. 1993. PMID: 8313624

7

Nonsyndromic hearing impairment is associated with a mutation in DFNA5.

Van Laer L, Huizing EH, Verstreken M, van Zuijlen D, Wauters JG, Bossuyt PJ, Van de Heyning P, McGuirt WT, Smith RJ, Willems PJ, Legan PK, Richardson GP, Van Camp G. Van Laer L, et al. Among authors: bossuyt pj. Nat Genet. 1998 Oct;20(2):194-7. doi: 10.1038/2503. Nat Genet. 1998. PMID: 9771715

8

Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mapping.

Mathysen D, Wuyts W, Bossuyt PJ, Wauters JG, Van Hul W. Mathysen D, et al. Among authors: bossuyt pj. Cytogenet Cell Genet. 2001;92(1-2):162-3. doi: 10.1159/000056890. Cytogenet Cell Genet. 2001. PMID: 11306818 No abstract available.

9

Incidence of low-fluorescence alpha satellite region on chromosome 21 escaping detection of aneuploidy at interphase by FISH.

Bossuyt PJ, Van Tienen MN, De Gruyter L, Smets V, Dumon J, Wauters JG. Bossuyt PJ, et al. Cytogenet Cell Genet. 1995;68(3-4):203-6. doi: 10.1159/000133914. Cytogenet Cell Genet. 1995. PMID: 7842737

10

Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31----q32.

Coucke P, Mangelschots K, Speleman F, Bossuyt P, Van Oostveldt P, Van der Auwera B, Carritt B, Willems PJ. Coucke P, et al. Among authors: bossuyt p. Cytogenet Cell Genet. 1991;57(2-3):120-2. doi: 10.1159/000133129. Cytogenet Cell Genet. 1991. PMID: 1914520

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