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Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder. [electronic resource] by
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Apolipoprotein E genotype in patients with Alzheimer's disease: implications for the risk of dementia among relatives. [electronic resource] by
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Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. [electronic resource] by
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[Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia]. [electronic resource] by
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- Bychkov, I Iu
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- Pogozheva, I V
- Fedotov, F F
- Soyan, G V
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In:
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Evidence for topologically protected surface states and a superconducting phase in [Tl4](Tl(1-x)Sn(x))Te3 using photoemission, specific heat, and magnetization measurements, and density functional theory. [electronic resource] by
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- Wen, J-J
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Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations. [electronic resource] by
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- De Stefano, G
- Rickards, O
- Martinez-Labarga, C
- Modiano, D
- Biondi, G
- Moral, P
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Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy. [electronic resource] by
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- Chabrol, B
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- Azulay, J P
- Attarian, S
- Pellissier, J F
- Gargus, J J
- Abdenur, J E
- Mozaffar, T
- Calvas, P
- Labauge, P
- Pages, M
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In:
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Differential structuring of human populations for homologous X and Y microsatellite loci. [electronic resource] by
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- Torroni, A
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- Wallace, D C
- Kidd, K K
- Olckers, A
- Moral, P
- Terrenato, L
- Akar, N
- Qamar, R
- Mansoor, A
- Mehdi, S Q
- Meloni, G
- Vona, G
- Cole, D E
- Cai, W
- Novelletto, A
Producer: 19971022
In:
American journal of human genetics vol. 61
Availability: No items available.
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