Speleman F - Search Results

1

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.

Menten B, Maas N, Thienpont B, Buysse K, Vandesompele J, Melotte C, de Ravel T, Van Vooren S, Balikova I, Backx L, Janssens S, De Paepe A, De Moor B, Moreau Y, Marynen P, Fryns JP, Mortier G, Devriendt K, Speleman F, Vermeesch JR. Menten B, et al. Among authors: speleman f. J Med Genet. 2006 Aug;43(8):625-33. doi: 10.1136/jmg.2005.039453. Epub 2006 Feb 20. J Med Genet. 2006. PMID: 16490798 Free PMC article.

2

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.

van Bon BW, Mefford HC, Menten B, Koolen DA, Sharp AJ, Nillesen WM, Innis JW, de Ravel TJ, Mercer CL, Fichera M, Stewart H, Connell LE, Ounap K, Lachlan K, Castle B, Van der Aa N, van Ravenswaaij C, Nobrega MA, Serra-Juhé C, Simonic I, de Leeuw N, Pfundt R, Bongers EM, Baker C, Finnemore P, Huang S, Maloney VK, Crolla JA, van Kalmthout M, Elia M, Vandeweyer G, Fryns JP, Janssens S, Foulds N, Reitano S, Smith K, Parkel S, Loeys B, Woods CG, Oostra A, Speleman F, Pereira AC, Kurg A, Willatt L, Knight SJ, Vermeesch JR, Romano C, Barber JC, Mortier G, Pérez-Jurado LA, Kooy F, Brunner HG, Eichler EE, Kleefstra T, de Vries BB. van Bon BW, et al. Among authors: speleman f. J Med Genet. 2009 Aug;46(8):511-23. doi: 10.1136/jmg.2008.063412. Epub 2009 Apr 15. J Med Genet. 2009. PMID: 19372089 Free PMC article.

3

Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization.

Speleman F, Leroy JG, Van Roy N, De Paepe A, Suijkerbuijk R, Brunner H, Looijenga L, Verschraegen-Spae MR, Orye E. Speleman F, et al. Am J Med Genet. 1991 Dec 1;41(3):381-7. doi: 10.1002/ajmg.1320410321. Am J Med Genet. 1991. PMID: 1789295

4

Interstitial telomeric sequences at the junction site of a jumping translocation.

Vermeesch JR, Petit P, Speleman F, Devriendt K, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: speleman f. Hum Genet. 1997 Jun;99(6):735-7. doi: 10.1007/s004390050440. Hum Genet. 1997. PMID: 9187665

5

Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines.

Van Roy N, Jauch A, Van Gele M, Laureys G, Versteeg R, De Paepe A, Cremer T, Speleman F. Van Roy N, et al. Among authors: speleman f. Cancer Genet Cytogenet. 1997 Sep;97(2):135-42. doi: 10.1016/s0165-4608(96)00362-7. Cancer Genet Cytogenet. 1997. PMID: 9283597

6

Assignment of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, De Paepe A, Messiaen L. De Baere E, et al. Among authors: speleman f. Cytogenet Cell Genet. 1998;82(3-4):226-7. doi: 10.1159/000015107. Cytogenet Cell Genet. 1998. PMID: 9858824 No abstract available.

7

Assignment of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25-->q26.1 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, De Paepe A, Messiaen L. De Baere E, et al. Among authors: speleman f. Cytogenet Cell Genet. 1998;82(3-4):228-9. doi: 10.1159/000015108. Cytogenet Cell Genet. 1998. PMID: 9858825 No abstract available.

8

Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, Mortier K, De Paepe A, Messiaen L. De Baere E, et al. Among authors: speleman f. Cytogenet Cell Genet. 1998;83(3-4):240-1. doi: 10.1159/000015191. Cytogenet Cell Genet. 1998. PMID: 10072590 No abstract available.

9

Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines.

Van Roy N, Van Limbergen H, Vandesompele J, Van Gele M, Poppe B, Laureys G, De Paepe A, Speleman F. Van Roy N, et al. Among authors: speleman f. Med Pediatr Oncol. 2000 Dec;35(6):538-40. doi: 10.1002/1096-911x(20001201)35:6<538::aid-mpo8>3.0.co;2-c. Med Pediatr Oncol. 2000. PMID: 11107111

10

Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies.

Poppe B, Van Limbergen H, Van Roy N, Vandecruys E, De Paepe A, Benoit Y, Speleman F. Poppe B, et al. Among authors: speleman f. Cancer Genet Cytogenet. 2001 Jul 1;128(1):39-42. doi: 10.1016/s0165-4608(01)00392-2. Cancer Genet Cytogenet. 2001. PMID: 11454428

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