Devi Akela | Diagnostics Division Centre For Dna Fingerprinting And Diagnostics
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概要
- Devi Akela Radha Ramaの詳細を見る
- 同名の論文著者
- Diagnostics Division Centre For Dna Fingerprinting And Diagnosticsの論文著者
関連著者
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Savithri Gorinabele
Laboratory Of Molecular And Cellular Biology Centre For Dna Fingerprinting And Diagnostics (cdfd)
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Devi Akela
Diagnostics Division Centre For Dna Fingerprinting And Diagnostics
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GOPIKRISHNA Munimanda
National Genomics and Transcriptomics Facility, Centre for DNA Fingerprinting and Diagnostics
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Gopikrishna Munimanda
National Genomics And Transcriptomics Facility Centre For Dna Fingerprinting And Diagnostics
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Bashyam M
National Genomics And Transcriptomics Facility Centre For Dna Fingerprinting And Diagnostics (cdfd)
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Bashyam Murali
Laboratory Of Molecular Oncology Centre For Dna Fingerprinting And Diagnostics
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Savithri G
Laboratory Of Molecular And Cellular Biology Centre For Dna Fingerprinting And Diagnostics (cdfd)
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Savithri Gorinabele
Laboratory Of Molecular Oncology Centre For Dna Fingerprinting And Diagnostics
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Devi Akela
インド
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RATHEESH Raman
Laboratory of Molecular Oncology, Centre for DNA Fingerprinting and Diagnostics
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SWARNALATA Gowrishankar
Apollo hospitals
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BASHYAM Murali
National Genomics and Transcriptomics Facility, Centre for DNA Fingerprinting and Diagnostics (CDFD)
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BASHYAM Leena
Diagnostics division, Centre for DNA Fingerprinting and Diagnostics (CDFD)
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SANGAL Vartul
National Genomics and Transcriptomics Facility, Centre for DNA Fingerprinting and Diagnostics (CDFD)
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Sangal Vartul
National Genomics And Transcriptomics Facility Centre For Dna Fingerprinting And Diagnostics (cdfd)
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Bashyam Leena
Diagnostics Division Centre For Dna Fingerprinting And Diagnostics (cdfd)
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Ratheesh Raman
Laboratory Of Molecular Oncology Centre For Dna Fingerprinting And Diagnostics
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GOPIKRISHNA Munimanda
National Genomics and Transcriptomics Facility, Centre for DNA Fingerprinting and Diagnostics (CDFD)
著作論文
- Farber lipogranulomatosis : clinical and molecular genetic analysis reveals a novel mutation in an Indian family
- Molecular genetic analyses of β-thalassemia in South India reveals rare mutations in the β-globin gene