DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray : standardization of molecular investigations of genetic diseases due to consanguinity
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概要
- 論文の詳細を見る
- Springer Japanの論文
- 2007-01-01
著者
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Tang Hoi-yin
Prenatal Diagnosis And Counseling Department Tsan Yuk Hospital
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Lam Ching-wan
Department Of Chemical Pathology The Chinese University Of Hong Kong Prince Of Wales Hospital
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Lam Ching-wan
Department Of Chemical Pathology Prince Of Wales Hospital The Chinese University Of Hong Kong
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Chan Michael
Department Of Chemical Pathology The Chinese University Of Hong Kong Prince Of Wales Hospital
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TONG Sui-Fan
Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital
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Tong Sui-fan
Department Of Chemical Pathology The Chinese University Of Hong Kong Prince Of Wales Hospital
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WONG Keong
Department of Obstetrics and Gynecology, Centro Hospitalar Conde S. Januario
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LUO Y.
Department of Obstetrics and Gynecology, Centro Hospitalar Conde S. Januario
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HA Shau-Yin
Department of Pediatrics and Adolescent Medicine, The University of Hong Kong, Queen Mary Hospital
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Wong Keong
Department Of Obstetrics And Gynecology Centro Hospitalar Conde S. Januario
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Ha Shau-yin
Department Of Pediatrics And Adolescent Medicine The University Of Hong Kong Queen Mary Hospital
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Lam Ching-wan
Chinese Univ. Hong Kong Hong Kong Chn
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Tong Sui‐fan
Chinese Univ. Hong Kong Hong Kong Chn
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Luo Y.
Department Of Obstetrics And Gynecology Centro Hospitalar Conde S. Januario
関連論文
- Management of Massive Hemoptysis : A Single Institution Experience
- Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese : Identification of 17 novel mutations and its genetic heterogeneity
- Mutational Study of ATP7B in Wilson Disease : Establishing an Effective DNA-based Diagnostic Protocol for Hong Kong Chinese
- DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray : standardization of molecular investigations of genetic diseases due to consanguinity
- Functional deficiencies of sulfite oxidase : Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia
- Fatal viral infection-associated encephalopathy in two Chinese boys : a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants
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