E P Economou - JoVE Visualize

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American Journal of Medical Genetics|January 15, 1992

Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathyD P Zhu, E P Economou, S E Antonarakis, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990

The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genomeE P Economou, A W Bergen, A C Warren, et al.

Genomics|May 1, 1990

Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic markerM B Petersen, E P Economou, S A Slaugenhaupt, et al.

Blood|January 11, 1991

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regionsE P Economou, S E Antonarakis, H H Kazazian, et al.

American Journal of Human Genetics|January 1, 1991

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndromeM B Petersen, A A Schinzel, F Binkert, et al.

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Showing results (1-10 of 5) with videos related to

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Pageof 1

American Journal of Medical Genetics|January 15, 1992

Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathyD P Zhu, E P Economou, S E Antonarakis, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990

The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genomeE P Economou, A W Bergen, A C Warren, et al.

Genomics|May 1, 1990

Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic markerM B Petersen, E P Economou, S A Slaugenhaupt, et al.

Blood|January 11, 1991

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regionsE P Economou, S E Antonarakis, H H Kazazian, et al.

American Journal of Human Genetics|January 1, 1991

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndromeM B Petersen, A A Schinzel, F Binkert, et al.

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