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B. Wieringa
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Journal Articles

Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35→q36.1 and identification of an intragenic genetic marker

Subject Area:
Genetics
A.M.J.M. van den Maagdenberg, D. Olde Weghuis, J. Rijss, R.A.C. van de Wetering, B. Wieringa, A. Geurts van Kessel, W.J.A.J. Hendriks
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1996) 73 (1-2): 145–148.
https://doi.org/10.1159/000134327
Published Online: 20 May 2008
View article titled, Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35→q36.1 and identification of an intragenic genetic marker
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Journal Articles

The gene (PTPN13) encoding the protein tyrosine phosphatase PTP-BL/PTP-BAS is located in mouse chromosome region 5E/F and human chromosome region 4q21

Subject Area:
Genetics
A.M.J.M. Van den Maagdenberg, D. Olde Weghuis, J. Rijss, G.F. Merkx, B. Wieringa, A. Geurts van Kessel, W.J.A.J. Hendriks
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1996) 74 (1-2): 153–155.
https://doi.org/10.1159/000134405
Published Online: 20 May 2008
View article titled, The gene (PTPN13) encoding the protein tyrosine phosphatase PTP-BL/PTP-BAS is located in mouse chromosome region 5E/F and human chromosome region 4q21
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Journal Articles

Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12→q13

Subject Area:
Genetics
P.M.T. Deen, D.O. Weghuis, R.J. Sinke, A. Geurts van Kessel, B. Wieringa, C.H. van Os
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1994) 66 (4): 260–262.
https://doi.org/10.1159/000133707
Published Online: 15 May 2008
View article titled, Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12→q13
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Journal Articles

Localization of the γ-subunit of the skeletal muscle L-type voltage-dependent calcium channel gene (CACNLG) to human chromosome band 17q24 by in situ hybridization and identification of a polymorphic repetitive DNA sequence at the gene locus

Subject Area:
Genetics
D.E. Iles, B. Segers, D. Olde Weghuis, R. Suikerbuijk, B. Wieringa
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1993) 64 (3-4): 227–230.
https://doi.org/10.1159/000133583
Published Online: 14 May 2008
View article titled, Localization of the γ-subunit of the skeletal muscle L-type voltage-dependent calcium channel gene (CACNLG) to human chromosome band 17q24 by in situ hybridization and identification of a polymorphic repetitive DNA sequence at the gene locus
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Journal Articles

The human gene for water channel aquaporin 1 (AQP1) is localized on chromosome 7p15→p14

Subject Area:
Genetics
P.M.T. Deen, D.O. Weghuis, A. Geurts van Kessel, B. Wieringa, C.H. van Os
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1994) 65 (4): 243–246.
https://doi.org/10.1159/000133639
Published Online: 14 May 2008
View article titled, The human gene for water channel aquaporin 1 (AQP1) is localized on chromosome 7p15→p14
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Journal Articles

Regional localization of the gene encoding pregnancy specific beta-1-glycoprotein 1 (PSBG1) to human chromosome 19q13.1

Subject Area:
Genetics
S.C. Niemann, D. Schonk, P. van Dijk, B. Wieringa, K.-H. Grzeschik, I. Bartels
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1989) 52 (1-2): 95–97.
https://doi.org/10.1159/000132851
Published Online: 13 May 2008
View article titled, Regional localization of the gene encoding pregnancy specific beta-1-glycoprotein 1 (PSBG1) to human chromosome 19q13.1
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Journal Articles

Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region

Subject Area:
Genetics
D. Schonk, P. van Dijk, P. Riegmann, J. Trapman, C. Holm, T.C. Willcocks, P. Sillekens, W. van Venrooij, E. Wimmer, A.G. Geurts van Kessel, H.-H. Ropers, B. Wieringa
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1990) 54 (1-2): 15–19.
https://doi.org/10.1159/000132946
Published Online: 13 May 2008
View article titled, Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region
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Journal Articles

Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19

Subject Area:
Genetics
T. Hulsebos, D. Schonk, I. van Dalen, M. Coerwinkel-Driessen, J. Schepens, H.H. Ropers, B. Wieringa
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1988) 47 (3): 144–148.
https://doi.org/10.1159/000132533
Published Online: 09 May 2008
View article titled, Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19
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Journal Articles

Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome

Subject Area:
Genetics
T. Hulsebos, B. Wieringa, R. Hochstenbach, D. Smeets, J. Schepens, F. Oerlemans, J. Zimmer, H.-H. Ropers
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1986) 43 (1-2): 47–56.
https://doi.org/10.1159/000132297
Published Online: 08 May 2008
View article titled, Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome
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Journal Articles

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

Subject Area:
Genetics
A. Gal, B. Wieringa, D.F.C.M. Smeets, L. Bleeker-Wagemakers, H.H. Ropers
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1986) 42 (4): 219–224.
https://doi.org/10.1159/000132282
Published Online: 08 May 2008
View article titled, Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease
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Journal Articles

Transgenic mouse models for myotonic dystrophy type 1 (DM1)

Subject Area:
Genetics
D.G. Wansink, B. Wieringa
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2003) 100 (1-4): 230–242.
https://doi.org/10.1159/000072859
Published Online: 15 October 2003
View article titled, Transgenic mouse models for myotonic dystrophy type 1 (DM1)
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Journal Articles

Assignment of the PTP-SL/PTPBR7 gene ( Ptprr /PTPRR) to mouse chromosome region 8A2 by in situ hybridization

Subject Area:
Genetics
A.M.J.M. van den Maagdenberg, J.T.G. Schepens, M.T.M. Schepens, G.F. Merkx, F. Darroudi, B. Wieringa, A. Geurts van Kessel, W.J.A.J. Hendriks
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1999) 84 (3-4): 243–244.
https://doi.org/10.1159/000015268
Published Online: 14 June 1999
View article titled, Assignment of the PTP-SL/PTPBR7 gene ( Ptprr /PTPRR) to mouse chromosome region 8A2 by in situ hybridization
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Journal Articles

Assignment of Ptprn2 , the gene encoding receptor-type protein tyrosine phosphatase IA-2β, a major autoantigen in insulin-dependent diabetes mellitus, to mouse chromosome region 12F

Subject Area:
Genetics
A.M.J.M. van den Maagdenberg, J.T.G. Schepens, M.T.M. Schepens, B. Pepers, B. Wieringa, A.Geurts Geurts van Kessel, W.J.A.J. Hendriks
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (1998) 82 (3-4): 153–155.
https://doi.org/10.1159/000015090
Published Online: 16 December 1998
View article titled, Assignment of Ptprn2 , the gene encoding receptor-type protein tyrosine phosphatase IA-2β, a major autoantigen in insulin-dependent diabetes mellitus, to mouse chromosome region 12F
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