Mangelschots K - 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. Hum Genet. 1992 Jun;89(4):407-13. doi: 10.1007/BF00194312. Hum Genet. 1992. PMID: 1352272

2

Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

Speleman F, Van der Auwera B, Mangelschots K, Vercruyssen M, Raap T, Wiegant J, Craen M, Leroy J. Speleman F, et al. Among authors: mangelschots k. Hum Genet. 1990 Oct;85(6):569-75. doi: 10.1007/BF00193576. Hum Genet. 1990. PMID: 2227946

3

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: mangelschots k. Hum Genet. 1993 Jan;90(5):489-95. doi: 10.1007/BF00217446. Hum Genet. 1993. PMID: 8094063

4

Improved immunocytochemical detection of biotinylated probes with Neutralite avidin.

van Roy N, Mangelschots K, Speleman F. van Roy N, et al. Among authors: mangelschots k. Trends Genet. 1993 Mar;9(3):71-2. doi: 10.1016/0168-9525(93)90217-6. Trends Genet. 1993. PMID: 8488564 No abstract available.

5

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: mangelschots k. Hum Genet. 1996 Mar;97(3):294-8. doi: 10.1007/BF02185757. Hum Genet. 1996. PMID: 8786067 Free article.

6

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

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

7

Analysis of whole-arm translocations in malignant blood cells by nonisotopic in situ hybridization.

Speleman F, Mangelschots K, Vercruyssen M, Dal Cin P, Aventin A, Offner F, Laureys G, Van den Berghe H, Leroy J. Speleman F, et al. Among authors: mangelschots k. Cytogenet Cell Genet. 1991;56(1):14-7. doi: 10.1159/000133036. Cytogenet Cell Genet. 1991. PMID: 2004549

8

Clinical profile of Angelman syndrome at different ages.

Buntinx IM, Hennekam RC, Brouwer OF, Stroink H, Beuten J, Mangelschots K, Fryns JP. Buntinx IM, et al. Among authors: mangelschots k. Am J Med Genet. 1995 Mar 27;56(2):176-83. doi: 10.1002/ajmg.1320560213. Am J Med Genet. 1995. PMID: 7625442

9

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: mangelschots k. Cytogenet Cell Genet. 1991;57(2-3):120-2. doi: 10.1159/000133129. Cytogenet Cell Genet. 1991. PMID: 1914520

10

i(12p) in a malignant ovarian tumor.

Speleman F, De Potter C, Dal Cin P, Mangelschots K, Ingelaere H, Laureys G, Benoit Y, Leroy J, Van Den Berghe H. Speleman F, et al. Among authors: mangelschots k. Cancer Genet Cytogenet. 1990 Mar;45(1):49-53. doi: 10.1016/0165-4608(90)90065-i. Cancer Genet Cytogenet. 1990. PMID: 2302685

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