Sethi Sidharth | Division Of Pediatric Nephrology And Genetics Department Of Pediatrics All India Institute Of Medica
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概要
- SETHI Sidharth Kumarの詳細を見る
- 同名の論文著者
- Division Of Pediatric Nephrology And Genetics Department Of Pediatrics All India Institute Of Medicaの論文著者
関連著者
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Bagga Arvind
Division Of Pediatric Nephrology And Genetics Department Of Pediatrics All India Institute Of Medica
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Sethi Sidharth
Division Of Pediatric Nephrology And Genetics Department Of Pediatrics All India Institute Of Medica
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DEKA Deepika
Department of Obstetrics and Gynecology, All India Institute of Medical Sciences
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Deka Deepika
Department Of Obstetrics And Gynaecology All India Institute Of Medical Sciences
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Lunardi Joel
Laboratoire De Biochimie Et Genetique Moleculaire
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SETHI Sidharth
Division of Pediatric Nephrology and Genetics, Department of Pediatrics, All India Institute of Medi
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KABRA Madhulika
Division of Pediatric Nephrology and Genetics, Department of Pediatrics, All India Institute of Medi
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BAGGA Arvind
Division of Pediatric Nephrology and Genetics, Department of Pediatrics, All India Institute of Medi
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Kabra Madhulika
Division Of Pediatric Nephrology And Genetics Department Of Pediatrics All India Institute Of Medica
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Bagga Arvind
All India Inst. Medical Sci. New Delhi Ind
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Sethi Sidharth
All India Inst. Medical Sci. New Delhi Ind
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MARIE-AGNES Dragon-Durey
Laboratoire d'Immunologie, Hopital Europeen Georges Pompidou, Universite Paris Descartes
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THAKER Neelam
Division of Pediatric Nephrology, Department of Pediatrics, All India Institute of Medical Sciences
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HARI Pankaj
Division of Pediatric Nephrology, Department of Pediatrics, All India Institute of Medical Sciences
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Hari Pankaj
Division Of Pediatric Nephrology Department Of Pediatrics All India Institute Of Medical Sciences
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Thaker Neelam
Division Of Pediatric Nephrology Department Of Pediatrics All India Institute Of Medical Sciences
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Marie-agnes Dragon-durey
Laboratoire D'immunologie Hopital Europeen Georges Pompidou Universite Paris Descartes
著作論文
- Antenatal diagnosis of Lowe syndrome
- Hemolytic uremic syndrome due to homozygous factor H deficiency