Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci
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概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2012-02-01
著者
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Nordenskjold Agneta
Department Of Molecular Medicine And Surgery Karolinska Institutet
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Gardiner Mark
General And Adolescent Paediatric Unit Institute Of Child Health University College London
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Chung Eddie
General And Adolescent Paediatric Unit Institute Of Child Health University College London
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Persson Sofia
Department Of Molecular Medicine And Surgery Karolinska Institutet
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Nordenskjold Agneta
Department Of Pediatric Surgery Astrid Lindgren Children's Hospital
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SVENNINGSSON Anna
Department of Molecular Medicine and Surgery, Karolinska Institutet
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SODERHALL Cilla
Department of Molecular Medicine and Surgery, Karolinska Institutet
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LUNDBERG Fredrik
Department of Molecular Medicine and Surgery, Karolinska Institutet
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LUTHMAN Holger
Department of Clinical Sciences, Malmo, Lund University
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KOCKUM Ingrid
Department of Clinical Neuroscience, Karolinska Institutet
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Luthman Holger
Department Of Clinical Sciences Malmo Lund University
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Soderhall Cilla
Department Of Molecular Medicine And Surgery Karolinska Institutet
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Lundberg Fredrik
Department Of Molecular Medicine And Surgery Karolinska Institutet
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Svenningsson Anna
Department Of Molecular Medicine And Surgery Karolinska Institutet
関連論文
- Increased Liver Enzymes in Adult Women with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndrome
- Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci
- No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric Stenosis