Author Search Results

1

P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal region by Wapenaar, M.C., Pearson, P.L., Van Ommen, G.J.B.

Published 1990

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2

Monoclonal antibodies for dystrophin analysis. Epitope mapping and improved binding to SDS-treated muscle sections. by Nguyen, T M, Ginjaar, I B, van Ommen, G J, Morris, G E

Published 1992

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3

Do human chromosomal bands 16p13 and 22q11-13 share ancestral origins? by Giles, R H, Dauwerse, H G, van Ommen, G J, Breuning, M H

Published 1998

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An alternative to FISH: detecting deletion and duplication carriers within 24 hours by White, S, Sterrenburg, E, van Ommen, G-J B, den Dunnen, J T, Breuning, M

Published 2003

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5

Alterations in immunoglobulin genes reveal the origin and evolution of monotypic and bitypic B cell lymphomas. by de Jong, D., Voetdijk, B. M., van Ommen, G. J., Kluin, P. M.

Published 1989

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6

RNA synthesis in isolated yeast mitochondria. by Groot, G S, van Harten-Loosbroek, N, van Ommen, G J, Pijst, H L

Published 1981

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7

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth. by Henke, A, Wapenaar, M, van Ommen, G J, Maraschio, P, Camerino, G, Rappold, G

Published 1991

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8

Behavioural complaints in participants who underwent predictive testing for Huntington's disease by Witjes-Ane, M, Zwinderman, A, Tibben, A, van Ommen, G-J B, Roos, R

Published 2002

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9

Fluorescent labelling of cRNA for microarray applications by ’t Hoen, Peter A. C., de Kort, Floor, van Ommen, G. J. B., den Dunnen, Johan T.

Published 2003

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10

The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kb. by Baas, F, van Ommen, G J, Bikker, H, Arnberg, A C, de Vijlder, J J

Published 1986

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11

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI. by Hofker, M H, Breuning, M H, Bakker, E, van Ommen, G J, Pearson, P L

Published 1985

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12

Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studies. by Bakker, E, Skraastad, M I, Fisser-Groen, Y M, van Ommen, G J, Pearson, P L

Published 1987

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13

RFLP for an anonymous single copy clone at 16pter-16p13.1 [D16S127] by Breuning, M H, Dauwerse, J G, Saris, J J, van Ommen, G J, Pearson, P L

Published 1989

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14

Duration of illness in Huntington's disease is not related to age at onset. by Roos, R A, Hermans, J, Vegter-van der Vlis, M, van Ommen, G J, Bruyn, G W

Published 1993

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15

Somatic changes in B-lymphoproliferative disorders (B-LPD) detected by DNA-fingerprinting. by de Jong, D., Voetdijk, B. M., Kluin-Nelemans, J. C., van Ommen, G. J., Kluin, P. M.

Published 1988

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16

Probe 218EP6 (D16S246) detects RFLP's close to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16 by Snijdewint, F.G.M., Saris, J.J., Dauwerse, J.G., Breuning, M.H., Van Ommen, G.J.B.

Published 1990

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17

Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame. by Nicholson, L V, Bushby, K M, Johnson, M A, den Dunnen, J T, Ginjaar, I B, van Ommen, G J

Published 1992

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18

Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product. by Datson, N A, van de Vosse, E, Dauwerse, H G, Bout, M, van Ommen, G J, den Dunnen, J T

Published 1996

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19

Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. by Breuning, M H, Snijdewint, F G, Dauwerse, J G, Saris, J J, Bakker, E, Pearson, P L, vanOmmen, G J

Published 1990

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20

A TaqI polymorphism identified by 26-6 (D16S125) proximal to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16 by Breuning, M.H., Snijdewint, F.G.M., Smits, J.R., Dauwerse, J.G., Saris, J.J., Van Ommen, G.J.B.

Published 1990

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Search Results - van Ommen, G. J.

P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal region by Wapenaar, M.C., Pearson, P.L., Van Ommen, G.J.B.

Monoclonal antibodies for dystrophin analysis. Epitope mapping and improved binding to SDS-treated muscle sections. by Nguyen, T M, Ginjaar, I B, van Ommen, G J, Morris, G E

Do human chromosomal bands 16p13 and 22q11-13 share ancestral origins? by Giles, R H, Dauwerse, H G, van Ommen, G J, Breuning, M H

An alternative to FISH: detecting deletion and duplication carriers within 24 hours by White, S, Sterrenburg, E, van Ommen, G-J B, den Dunnen, J T, Breuning, M

Alterations in immunoglobulin genes reveal the origin and evolution of monotypic and bitypic B cell lymphomas. by de Jong, D., Voetdijk, B. M., van Ommen, G. J., Kluin, P. M.

RNA synthesis in isolated yeast mitochondria. by Groot, G S, van Harten-Loosbroek, N, van Ommen, G J, Pijst, H L

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth. by Henke, A, Wapenaar, M, van Ommen, G J, Maraschio, P, Camerino, G, Rappold, G

Behavioural complaints in participants who underwent predictive testing for Huntington's disease by Witjes-Ane, M, Zwinderman, A, Tibben, A, van Ommen, G-J B, Roos, R

Fluorescent labelling of cRNA for microarray applications by ’t Hoen, Peter A. C., de Kort, Floor, van Ommen, G. J. B., den Dunnen, Johan T.

The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kb. by Baas, F, van Ommen, G J, Bikker, H, Arnberg, A C, de Vijlder, J J

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI. by Hofker, M H, Breuning, M H, Bakker, E, van Ommen, G J, Pearson, P L

Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studies. by Bakker, E, Skraastad, M I, Fisser-Groen, Y M, van Ommen, G J, Pearson, P L

RFLP for an anonymous single copy clone at 16pter-16p13.1 [D16S127] by Breuning, M H, Dauwerse, J G, Saris, J J, van Ommen, G J, Pearson, P L

Duration of illness in Huntington's disease is not related to age at onset. by Roos, R A, Hermans, J, Vegter-van der Vlis, M, van Ommen, G J, Bruyn, G W

Somatic changes in B-lymphoproliferative disorders (B-LPD) detected by DNA-fingerprinting. by de Jong, D., Voetdijk, B. M., Kluin-Nelemans, J. C., van Ommen, G. J., Kluin, P. M.

Probe 218EP6 (D16S246) detects RFLP's close to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16 by Snijdewint, F.G.M., Saris, J.J., Dauwerse, J.G., Breuning, M.H., Van Ommen, G.J.B.

Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame. by Nicholson, L V, Bushby, K M, Johnson, M A, den Dunnen, J T, Ginjaar, I B, van Ommen, G J

Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product. by Datson, N A, van de Vosse, E, Dauwerse, H G, Bout, M, van Ommen, G J, den Dunnen, J T

Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. by Breuning, M H, Snijdewint, F G, Dauwerse, J G, Saris, J J, Bakker, E, Pearson, P L, vanOmmen, G J

A TaqI polymorphism identified by 26-6 (D16S125) proximal to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16 by Breuning, M.H., Snijdewint, F.G.M., Smits, J.R., Dauwerse, J.G., Saris, J.J., Van Ommen, G.J.B.

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