Van Roy B - Search Results

1

Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Mangelschots K, Van Roy B, Speleman F, Van Roy N, Gheuens J, Beuten J, Buntinx I, Van Thienen MN, Willekens H, Dumon J, et al. Mangelschots K, et al. Among authors: van thienen mn, van roy b, van roy n. Hum Genet. 1992 Jun;89(4):407-13. doi: 10.1007/BF00194312. Hum Genet. 1992. PMID: 1352272

2

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: van roy b. Clin Genet. 1993 Nov;44(5):262-9. doi: 10.1111/j.1399-0004.1993.tb03894.x. Clin Genet. 1993. PMID: 8313624

3

Angelman syndrome in an inbred family.

Beuten J, Hennekam RC, Van Roy B, Mangelschots K, Sutcliffe JS, Halley DJ, Hennekam FA, Beaudet AL, Willems PJ. Beuten J, et al. Among authors: van roy b. Hum Genet. 1996 Mar;97(3):294-8. doi: 10.1007/BF02185757. Hum Genet. 1996. PMID: 8786067 Free article.

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: van der auwera bj. Am J Med Genet. 1990 May;36(1):122-5. doi: 10.1002/ajmg.1320360124. Am J Med Genet. 1990. PMID: 2333901

5

Tricho-rhino-phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24.

Marchau FE, Van Roy BC, Parizel PM, Lambert JR, De Canck I, Leroy JG, Gevaert CM, Willems PJ, Dumon JE. Marchau FE, et al. Among authors: van roy bc. Am J Med Genet. 1993 Feb 15;45(4):450-5. doi: 10.1002/ajmg.1320450411. Am J Med Genet. 1993. PMID: 8465849

6

Segregation of the fragile X mutation from an affected male to his normal daughter.

Willems PJ, Van Roy B, De Boulle K, Vits L, Reyniers E, Beck O, Dumon JE, Verkerk A, Oostra B. Willems PJ, et al. Among authors: van roy b. Hum Mol Genet. 1992 Oct;1(7):511-5. doi: 10.1093/hmg/1.7.511. Hum Mol Genet. 1992. PMID: 1307252

7

Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridisation.

Mangelschots K, Van Roy B, Buntinx I. Mangelschots K, et al. Among authors: van roy b. Clin Genet. 1991 Jul;40(1):62. doi: 10.1111/j.1399-0004.1991.tb03069.x. Clin Genet. 1991. PMID: 1884520 No abstract available.

8

Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms.

Stinissen P, Van Roy B, Van Camp G, Backhovens H, Partoens P, Wehnert A, Verniers H, Dumon J, Vandenberghe A, Van Broeckhoven C. Stinissen P, et al. Among authors: van roy b, van broeckhoven c, van camp g. Am J Med Genet Suppl. 1990;7:133-6. doi: 10.1002/ajmg.1320370727. Am J Med Genet Suppl. 1990. PMID: 1981473

9

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.

10

Antenatal ultrasonographic diagnosis of trisomy 18 (Edwards syndrome).

Stevens MJ, Dumon J, Jacquemyn Y, Van Roy B, Delbeke L, Gerris J, Buytaert P. Stevens MJ, et al. Among authors: van roy b. Eur J Obstet Gynecol Reprod Biol. 1987 Dec;26(4):353-8. doi: 10.1016/0028-2243(87)90134-1. Eur J Obstet Gynecol Reprod Biol. 1987. PMID: 3319733

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