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M C Wapenaar

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Journal of Neurology|December 1, 1989

Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.

Genomics|March 1, 1993

Isolation and mapping of human chromosome 21 cosmids using a probe for RTVL-H retrovirus-like elementsI Meulenbelt, M C Wapenaar, D Patterson, et al.

Vnitrni Lekarstvi|October 1, 1993

[Polymorphisms in the pseudoautosomal regions of X and Y in DNA diagnosis]Z Sieglová, M Mrug, M Láblerová, et al.

Cytogenetics and Cell Genetics|January 1, 1990

Isolation and characterization of cell hybrids containing human Xp-chromosome fragmentsM C Wapenaar, T Kievits, P Meera Khan, et al.

Clinical Genetics|April 1, 1989

Molecular deletions in the Duchenne/Becker muscular dystrophy geneK A Hart, S Abbs, M C Wapenaar, et al.

Human Genetics|January 1, 1985

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophyM H Hofker, M C Wapenaar, N Goor, et al.

Human Molecular Genetics|July 1, 1994

A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22M C Wapenaar, M V Schiaffino, M T Bassi, et al.

Cytometry|January 1, 1990

Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomesT Kievits, P Devilee, J Wiegant, et al.

American Journal of Medical Genetics|December 1, 1989

Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese femalesS Sugino, S Fujishita, N Kamimura, et al.

Human Molecular Genetics|July 1, 1993

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regionsM C Wapenaar, M T Bassi, L Schaefer, et al.

Pageof 3

Search research articles

Showing results (1-10 of 23) with videos related to

Sort By:

Pageof 3

Journal of Neurology|December 1, 1989

Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.

Genomics|March 1, 1993

Isolation and mapping of human chromosome 21 cosmids using a probe for RTVL-H retrovirus-like elementsI Meulenbelt, M C Wapenaar, D Patterson, et al.

Vnitrni Lekarstvi|October 1, 1993

[Polymorphisms in the pseudoautosomal regions of X and Y in DNA diagnosis]Z Sieglová, M Mrug, M Láblerová, et al.

Cytogenetics and Cell Genetics|January 1, 1990

Isolation and characterization of cell hybrids containing human Xp-chromosome fragmentsM C Wapenaar, T Kievits, P Meera Khan, et al.

Clinical Genetics|April 1, 1989

Molecular deletions in the Duchenne/Becker muscular dystrophy geneK A Hart, S Abbs, M C Wapenaar, et al.

Human Genetics|January 1, 1985

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophyM H Hofker, M C Wapenaar, N Goor, et al.

Human Molecular Genetics|July 1, 1994

A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22M C Wapenaar, M V Schiaffino, M T Bassi, et al.

Cytometry|January 1, 1990

Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomesT Kievits, P Devilee, J Wiegant, et al.

American Journal of Medical Genetics|December 1, 1989

Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese femalesS Sugino, S Fujishita, N Kamimura, et al.

Human Molecular Genetics|July 1, 1993

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regionsM C Wapenaar, M T Bassi, L Schaefer, et al.

Pageof 3