C D Boehm - JoVE Visualize

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Molecular Biology & Medicine|June 1, 1989

Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutationK J Hofman, S E Antonarakis, S Missiou-Tsangaraki, et al.

The New England Journal of Medicine|May 5, 1983

Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemiaC D Boehm, S E Antonarakis, J A Phillips, et al.

Progress in Clinical and Biological Research|January 1, 1983

Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutationsH H Kazazian, S E Antonarakis, T Cheng, et al.

Blood|April 1, 1986

Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian familyC D Boehm, C E Dowling, P G Waber, et al.

Nature Genetics|June 1, 1994

A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertionS E Holmes, B A Dombroski, C M Krebs, et al.

American Journal of Human Genetics|July 1, 1985

Evidence supporting a single origin of the beta(C)-globin gene in blacksC D Boehm, C E Dowling, S E Antonarakis, et al.

Molecular Genetics and Metabolism|March 9, 1999

Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophyC D Boehm, G R Cutting, M B Lachtermacher, et al.

American Journal of Human Genetics|September 1, 1983

beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin geneH H Kazazian, S H Orkin, C D Boehm, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 15, 1996

Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesisJ P Issa, P M Vertino, C D Boehm, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1986

On the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groupsC Wong, S E Antonarakis, S C Goff, et al.

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Showing results (11-20 of 35) with videos related to

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Pageof 4

Molecular Biology & Medicine|June 1, 1989

Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutationK J Hofman, S E Antonarakis, S Missiou-Tsangaraki, et al.

The New England Journal of Medicine|May 5, 1983

Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemiaC D Boehm, S E Antonarakis, J A Phillips, et al.

Progress in Clinical and Biological Research|January 1, 1983

Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutationsH H Kazazian, S E Antonarakis, T Cheng, et al.

Blood|April 1, 1986

Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian familyC D Boehm, C E Dowling, P G Waber, et al.

Nature Genetics|June 1, 1994

A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertionS E Holmes, B A Dombroski, C M Krebs, et al.

American Journal of Human Genetics|July 1, 1985

Evidence supporting a single origin of the beta(C)-globin gene in blacksC D Boehm, C E Dowling, S E Antonarakis, et al.

Molecular Genetics and Metabolism|March 9, 1999

Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophyC D Boehm, G R Cutting, M B Lachtermacher, et al.

American Journal of Human Genetics|September 1, 1983

beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin geneH H Kazazian, S H Orkin, C D Boehm, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 15, 1996

Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesisJ P Issa, P M Vertino, C D Boehm, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1986

On the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groupsC Wong, S E Antonarakis, S C Goff, et al.

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