Mannens M - Search Results

1

Identification of copy number variants associated with BPES-like phenotypes.

Gijsbers AC, D'haene B, Hilhorst-Hofstee Y, Mannens M, Albrecht B, Seidel J, Witt DR, Maisenbacher MK, Loeys B, van Essen T, Bakker E, Hennekam R, Breuning MH, De Baere E, Ruivenkamp CA. Gijsbers AC, et al. Among authors: mannens m. Hum Genet. 2008 Dec;124(5):489-98. doi: 10.1007/s00439-008-0574-9. Epub 2008 Oct 25. Hum Genet. 2008. PMID: 18953567

2

The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor.

van den Ouweland AM, Verdijk M, Mannens MM, van Oost BA. van den Ouweland AM, et al. Among authors: mannens mm. Hum Genet. 1992 Sep-Oct;90(1-2):144-6. doi: 10.1007/BF00210759. Hum Genet. 1992. PMID: 1330878

3

Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23.

Bout A, Hoovers JM, Bakker E, Mannens MM, Geurts van Kessel A, Westerveld A, Tager JM, Benne R. Bout A, et al. Among authors: mannens mm. Cytogenet Cell Genet. 1989;52(3-4):147-50. doi: 10.1159/000132865. Cytogenet Cell Genet. 1989. PMID: 2630187

4

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.

Mannens M, Slater RM, Heyting C, Bliek J, de Kraker J, Coad N, de Pagter-Holthuizen P, Pearson PL. Mannens M, et al. Hum Genet. 1988 Dec;81(1):41-8. doi: 10.1007/BF00283727. Hum Genet. 1988. PMID: 2848758

5

Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.

Fantes J, Redeker B, Breen M, Boyle S, Brown J, Fletcher J, Jones S, Bickmore W, Fukushima Y, Mannens M, et al. Fantes J, et al. Among authors: mannens m. Hum Mol Genet. 1995 Mar;4(3):415-22. doi: 10.1093/hmg/4.3.415. Hum Mol Genet. 1995. PMID: 7795596

6

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

Mannens M, Hoovers JM, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, Coad N, Steenman M, Bliek J, et al. Mannens M, et al. Eur J Hum Genet. 1994;2(1):3-23. doi: 10.1159/000472337. Eur J Hum Genet. 1994. PMID: 7913866

7

TaqI and RsaI polymorphisms in the H19 gene (D11S813E).

Redeker E, Van Moorsel CJ, Feinberg A, Mannens M. Redeker E, et al. Among authors: mannens m. Hum Mol Genet. 1993 Jun;2(6):823. doi: 10.1093/hmg/2.6.823. Hum Mol Genet. 1993. PMID: 8102574 No abstract available.

8

Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.

Fukushima Y, Hoovers J, Mannens M, Wakui K, Ohashi H, Ohno T, Ueoka Y, Niikawa N. Fukushima Y, et al. Among authors: mannens m. Hum Genet. 1993 Apr;91(3):205-9. doi: 10.1007/BF00218257. Hum Genet. 1993. PMID: 8478003

9

Further delineation of the partial proximal trisomy 10q syndrome.

Aalfs CM, Hoovers JM, Nieste-Otter MA, Mannens MM, Hennekam RC, Leschot NJ. Aalfs CM, et al. Among authors: mannens mm. J Med Genet. 1995 Dec;32(12):968-71. doi: 10.1136/jmg.32.12.968. J Med Genet. 1995. PMID: 8825926 Free PMC article.

10

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

Alders M, Ryan A, Hodges M, Bliek J, Feinberg AP, Privitera O, Westerveld A, Little PF, Mannens M. Alders M, et al. Among authors: mannens m. Am J Hum Genet. 2000 May;66(5):1473-84. doi: 10.1086/302892. Epub 2000 Apr 10. Am J Hum Genet. 2000. PMID: 10762538 Free PMC article.

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