SCHWARTZ Marianne | Department of Clinical Genetics, The Juliane Marie Centre, Copenhagen University Hospital
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概要
- SCHWARTZ Marianneの詳細を見る
- 同名の論文著者
- Department of Clinical Genetics, The Juliane Marie Centre, Copenhagen University Hospitalの論文著者
関連著者
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SCHWARTZ Marianne
Department of Clinical Genetics, The Juliane Marie Centre, Copenhagen University Hospital
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Schwartz Marianne
Department Of Clinical Genetics 4062 Rigshopitalet University Hospital
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Nielsen Jytte
Department Of Clinical Genetics 4062 Rigshopitalet University Hospital
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Kreiborg Sven
Department Of Pediatric Dentistry And Clinical Genetics School Of Dentistry
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KELLER Mette
Department of Pediatric Dentistry and Clinical Genetics, School of Dentistry
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HERMANN Nuno
Department of Pediatric Dentistry and Clinical Genetics, School of Dentistry
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DARVANN Tron
3D Laboratory, Faculty of Health Sciences, University of Copenhagen
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LARSEN Per
3D Laboratory, Faculty of Health Sciences, University of Copenhagen
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HOVE Hanne
Department of Clinical Genetics, The Juliane Marie Centre, Copenhagen University Hospital
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CHRISTENSEN Leif
Department of Neurosurgery, Aarhus University Hospital
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MARSH Jeffrey
Kids Plastic Surgery, St. John's Mercy Hospital
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Larsen Per
3d Laboratory Faculty Of Health Sciences University Of Copenhagen
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Hove Hanne
Department Of Clinical Genetics The Juliane Marie Centre Copenhagen University Hospital
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Hermann Nuno
Department Of Pediatric Dentistry And Clinical Genetics School Of Dentistry
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Darvann Tron
3d Laboratory Faculty Of Health Sciences University Of Copenhagen
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Keller Mette
Department Of Pediatric Dentistry And Clinical Genetics School Of Dentistry
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Marsh Jeffrey
Kids Plastic Surgery St. John's Mercy Hospital
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RAVN Kirstine
Department of Clinical Genetics, 4062, Rigshopitalet University Hospital
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Christensen Leif
Department Of Neurosurgery Aarhus University Hospital
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Ravn Kirstine
Department Of Clinical Genetics 4062 Rigshopitalet University Hospital
著作論文
- Craniofacial Morphology in Muenke Syndrome
- A 77-year-old woman and a preserved speech variant among the Danish Rett patients with mutations in MECP2