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Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
Zeidler, Claudia; Woelfle, Joachim; Draaken, Markus; Mughal, Sadaf S; Große, Greta; Hilger, Alina C; Dworschak, Gabriel C; Boemers, Thomas M; Jenetzky, Ekkehart; Zwink, Nadine; Lacher, Martin; Schmidt, Dominik; Schmiedeke, Eberhard; Grasshoff-Derr, Sabine; Märzheuser, Stefanie; Holland-Cunz, Stefan; Schäfer, Mattias; Bartels, Enrika; Keppler, Kathleen; Palta, Markus; Leonhardt, Johannes; Kujath, Christina; Rißmann, Anke; Nöthen, Markus M; Reutter, Heiko; Ludwig, Michael.
Affiliation
  • Zeidler C; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Bonn, Germany.
Birth Defects Res A Clin Mol Teratol ; 100(10): 750-9, 2014 Oct.
Article in En | MEDLINE | ID: mdl-25131394
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Anal Canal / Spine / Trachea / Limb Deformities, Congenital / Cryptorchidism / Esophagus / Fibroblast Growth Factor 8 / Heart Defects, Congenital / Kidney / Mutation Type of study: Prognostic_studies Limits: Humans / Male Country/Region as subject: Europa Language: En Journal: Birth Defects Res A Clin Mol Teratol Year: 2014 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Anal Canal / Spine / Trachea / Limb Deformities, Congenital / Cryptorchidism / Esophagus / Fibroblast Growth Factor 8 / Heart Defects, Congenital / Kidney / Mutation Type of study: Prognostic_studies Limits: Humans / Male Country/Region as subject: Europa Language: En Journal: Birth Defects Res A Clin Mol Teratol Year: 2014 Document type: Article Affiliation country: Country of publication: