Speleman F - Search Results

1

Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type.

Menten B, Buysse K, Vandesompele J, De Smet E, De Paepe A, Speleman F, Mortier G. Menten B, et al. Among authors: speleman f. Eur J Med Genet. 2005 Jul-Sep;48(3):301-9. doi: 10.1016/j.ejmg.2005.04.014. Eur J Med Genet. 2005. PMID: 16179225

2

Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH.

Van Limbergen H, Poppe B, Michaux L, Herens C, Brown J, Noens L, Berneman Z, De Bock R, De Paepe A, Speleman F. Van Limbergen H, et al. Among authors: speleman f. Genes Chromosomes Cancer. 2002 Jan;33(1):60-72. doi: 10.1002/gcc.1212. Genes Chromosomes Cancer. 2002. PMID: 11746988

3

Quantification of MYCN, DDX1, and NAG gene copy number in neuroblastoma using a real-time quantitative PCR assay.

De Preter K, Speleman F, Combaret V, Lunec J, Laureys G, Eussen BH, Francotte N, Board J, Pearson AD, De Paepe A, Van Roy N, Vandesompele J. De Preter K, et al. Among authors: speleman f. Mod Pathol. 2002 Feb;15(2):159-66. doi: 10.1038/modpathol.3880508. Mod Pathol. 2002. PMID: 11850545

4

Elimination of primer-dimer artifacts and genomic coamplification using a two-step SYBR green I real-time RT-PCR.

Vandesompele J, De Paepe A, Speleman F. Vandesompele J, et al. Among authors: speleman f. Anal Biochem. 2002 Apr 1;303(1):95-8. doi: 10.1006/abio.2001.5564. Anal Biochem. 2002. PMID: 11906156 No abstract available.

5

Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion.

Vermeulen S, Messiaen L, Scheir P, De Bie S, Speleman F, De Paepe A. Vermeulen S, et al. Among authors: speleman f. Am J Med Genet. 2002 Apr 1;108(4):315-8. doi: 10.1002/ajmg.10295. Am J Med Genet. 2002. PMID: 11920837

6

A brief commentary on "Chromosomal aberrations in neuroblastoma cell lines identified by cross species color banding and chromosome painting".

Vandesompele J, Speleman F. Vandesompele J, et al. Among authors: speleman f. Cancer Genet Cytogenet. 2002 Jun;135(2):196. doi: 10.1016/s0165-4608(01)00642-2. Cancer Genet Cytogenet. 2002. PMID: 12127407 No abstract available.

7

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes.

Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F. Vandesompele J, et al. Among authors: speleman f. Genome Biol. 2002 Jun 18;3(7):RESEARCH0034. doi: 10.1186/gb-2002-3-7-research0034. Epub 2002 Jun 18. Genome Biol. 2002. PMID: 12184808 Free PMC article.

8

Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.

Van Roy N, Vandesompele J, Berx G, Staes K, Van Gele M, De Smet E, De Paepe A, Laureys G, van der Drift P, Versteeg R, Van Roy F, Speleman F. Van Roy N, et al. Among authors: speleman f. Genes Chromosomes Cancer. 2002 Oct;35(2):113-20. doi: 10.1002/gcc.10034. Genes Chromosomes Cancer. 2002. PMID: 12203774

9

Combined karyotyping, CGH and M-FISH analysis allows detailed characterization of unidentified chromosomal rearrangements in Merkel cell carcinoma.

Van Gele M, Leonard JH, Van Roy N, Van Limbergen H, Van Belle S, Cocquyt V, Salwen H, De Paepe A, Speleman F. Van Gele M, et al. Among authors: speleman f. Int J Cancer. 2002 Sep 10;101(2):137-45. doi: 10.1002/ijc.10591. Int J Cancer. 2002. PMID: 12209990 Review.

10

RTPrimerDB: the real-time PCR primer and probe database.

Pattyn F, Speleman F, De Paepe A, Vandesompele J. Pattyn F, et al. Among authors: speleman f. Nucleic Acids Res. 2003 Jan 1;31(1):122-3. doi: 10.1093/nar/gkg011. Nucleic Acids Res. 2003. PMID: 12519963 Free PMC article.

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