Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-12-01
著者
-
Wong Lee-jun
Department Of Molecular And Human Genetics Baylor College Of Medicine
-
Hirano Michio
Department Of Neurology Columbia University College Of Physicians & Surgeons
-
Douglas Ganka
Department Of Molecular And Human Genetics Baylor College Of Medicine
-
WISZNIEWSKA Joanna
Department of Molecular and Human Genetics, Baylor College of Medicine
-
LIPSON Mark
Department of Genetics, Kaiser Permanente
-
WITT David
Department of Genetics, Kaiser Permanente
-
MCDOWELL Taryn
Department of Genetics, Kaiser Permanente
-
SIFRY-PLATT Mara
Department of Genetics, Kaiser Permanente
-
CRAIGEN William
Department of Molecular and Human Genetics, Baylor College of Medicine
-
Craigen William
Department Of Molecular And Human Genetics Baylor College Of Medicine
-
Hirano Michio
Department Of Neurology Columbia University Medical Center
-
Lipson Mark
Department Of Genetics Kaiser Permanente
-
Sifry-platt Mara
Department Of Genetics Kaiser Permanente
-
Mcdowell Taryn
Department Of Genetics Kaiser Permanente
関連論文
- First prenatal exclusion of cystic fibrosis in East Asia
- Biochemical and genetic analysis of Leigh syndrome patients in Korea
- Alpers syndrome with prominent white matter changes
- Benign cysts in the central nervous system : Neuropathological observations of the cyst walls
- Mitochondrial DNA variant interactions modify breast cancer risk
- Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis