van Ommen GJ - Search Results

1

Physical mapping of 14 new DNA markers isolated from the human distal Xp region.

Wapenaar MC, Petit C, Basler E, Ballabio A, Henke A, Rappold GA, van Paassen HM, Blonden LA, van Ommen GJ. Wapenaar MC, et al. Among authors: van paassen hm, van ommen gj. Genomics. 1992 May;13(1):167-75. doi: 10.1016/0888-7543(92)90217-g. Genomics. 1992. PMID: 1349572

2

Isolation and characterization of cell hybrids containing human Xp-chromosome fragments.

Wapenaar MC, Kievits T, Meera Khan P, Pearson PL, Van Ommen GJ. Wapenaar MC, et al. Among authors: van ommen gj. Cytogenet Cell Genet. 1990;54(1-2):10-4. doi: 10.1159/000132945. Cytogenet Cell Genet. 1990. PMID: 2249469

3

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.

Blonden LA, den Dunnen JT, van Paassen HM, Wapenaar MC, Grootscholten PM, Ginjaar HB, Bakker E, Pearson PL, van Ommen GJ. Blonden LA, et al. Among authors: van paassen hm, van ommen gj. Nucleic Acids Res. 1989 Jul 25;17(14):5611-21. doi: 10.1093/nar/17.14.5611. Nucleic Acids Res. 1989. PMID: 2569720 Free PMC article.

4

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Den Dunnen JT, Grootscholten PM, Bakker E, Blonden LA, Ginjaar HB, Wapenaar MC, van Paassen HM, van Broeckhoven C, Pearson PL, van Ommen GJ. Den Dunnen JT, et al. Among authors: van paassen hm, van ommen gj, van broeckhoven c. Am J Hum Genet. 1989 Dec;45(6):835-47. Am J Hum Genet. 1989. PMID: 2573997 Free PMC article.

5

Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library.

Driesen MS, Dauwerse JG, Wapenaar MC, Meershoek EJ, Mollevanger P, Chen KL, Fischbeck KH, van Ommen GJ. Driesen MS, et al. Among authors: van ommen gj. Genomics. 1991 Dec;11(4):1079-87. doi: 10.1016/0888-7543(91)90035-d. Genomics. 1991. PMID: 1783377

6

Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes.

Kievits T, Devilee P, Wiegant J, Wapenaar MC, Cornelisse CJ, van Ommen GJ, Pearson PL. Kievits T, et al. Among authors: van ommen gj. Cytometry. 1990;11(1):105-9. doi: 10.1002/cyto.990110112. Cytometry. 1990. PMID: 2307050 Free article.

7

A polymorphic STS in intron 44 of the dystrophin gene.

Blonden LA, Terwindt GM, Den Dunnen JT, Van Ommen GJ. Blonden LA, et al. Among authors: van ommen gj. Hum Genet. 1994 Apr;93(4):479-80. doi: 10.1007/BF00201683. Hum Genet. 1994. PMID: 7909532

8

AK1 detects a VNTR locus in the pseudoautosomal region.

Klink A, Wapenaar M, van Ommen GJ, Rappold G. Klink A, et al. Among authors: van ommen gj. Hum Mol Genet. 1993 Mar;2(3):339. doi: 10.1093/hmg/2.3.339-a. Hum Mol Genet. 1993. PMID: 8098983 No abstract available.

9

A CA-repeat polymorphism near DXS418 (P122).

Van De Vosse E, Booms PF, Vossen RH, Wapenaar MC, Van Ommen GJ, Den Dunnen JT. Van De Vosse E, et al. Among authors: van ommen gj. Hum Mol Genet. 1993 Dec;2(12):2202. doi: 10.1093/hmg/2.12.2202-a. Hum Mol Genet. 1993. PMID: 8111402 No abstract available.

10

A high resolution deletion map of human chromosome Xp22.

Schaefer L, Ferrero GB, Grillo A, Bassi MT, Roth EJ, Wapenaar MC, van Ommen GJ, Mohandas TK, Rocchi M, Zoghbi HY, Ballabio A. Schaefer L, et al. Among authors: van ommen gj. Nat Genet. 1993 Jul;4(3):272-9. doi: 10.1038/ng0793-272. Nat Genet. 1993. PMID: 8358436

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