Mannens M - Search Results

1

High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.

Hoovers JM, Redeker E, Speleman F, Höppener JW, Bhola S, Bliek J, van Roy N, Leschot NJ, Westerveld A, Mannens M. Hoovers JM, et al. Among authors: mannens m. Genomics. 1993 Mar;15(3):525-9. doi: 10.1006/geno.1993.1104. Genomics. 1993. PMID: 8468047

2

Imprinting and Beckwith-Wiedemann syndrome.

Hoovers JM, Dietrich AJ, Mannens MM. Hoovers JM, et al. Among authors: mannens mm. Lancet. 1992 May 16;339(8803):1228. doi: 10.1016/0140-6736(92)91164-4. Lancet. 1992. PMID: 1349953 No abstract available.

3

The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.

Heding IJ, Ivens AC, Wilson J, Strivens M, Gregory S, Hoovers JM, Mannens M, Redeker B, Porteous D, van Heyningen V, et al. Heding IJ, et al. Among authors: mannens m. Genomics. 1992 May;13(1):89-94. doi: 10.1016/0888-7543(92)90206-8. Genomics. 1992. PMID: 1577496

4

Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood.

Devilee P, van den Broek M, Mannens M, Slater R, Cornelisse CJ, Westerveld A, Khan PM. Devilee P, et al. Among authors: mannens m. Int J Cancer. 1991 Apr 1;47(6):817-21. doi: 10.1002/ijc.2910470604. Int J Cancer. 1991. PMID: 1672665

5

High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.

Hoovers JM, Mannens M, John R, Bliek J, van Heyningen V, Porteous DJ, Leschot NJ, Westerveld A, Little PF. Hoovers JM, et al. Among authors: mannens m. Genomics. 1992 Feb;12(2):254-63. doi: 10.1016/0888-7543(92)90372-y. Genomics. 1992. PMID: 1740334

6

The distal region of 11p13 and associated genetic diseases.

Mannens M, Hoovers JM, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heyningen V, Junien C, et al. Mannens M, et al. Genomics. 1991 Oct;11(2):284-93. doi: 10.1016/0888-7543(91)90134-z. Genomics. 1991. PMID: 1769647

7

Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization.

Speleman F, Mannens M, Redeker B, Vercruyssen M, Van Oostveldt P, Leroy J, Slater R. Speleman F, et al. Among authors: mannens m. Cytogenet Cell Genet. 1991;56(3-4):129-31. doi: 10.1159/000133068. Cytogenet Cell Genet. 1991. PMID: 2055105

8

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.

Mannens M, Devilee P, Bliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A. Mannens M, et al. Cancer Res. 1990 Jun 1;50(11):3279-83. Cancer Res. 1990. PMID: 2159377

9

Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.

Mannens M, Bleeker-Wagemakers EM, Bliek J, Hoovers J, Mandjes I, van Tol S, Frants RR, Heyting C, Westerveld A, Slater RM. Mannens M, et al. Cytogenet Cell Genet. 1989;52(1-2):32-6. doi: 10.1159/000132834. Cytogenet Cell Genet. 1989. PMID: 2575483

10

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

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