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Journal of Pediatric Gastroenterology and Nutrition|February 3, 2016
Congenital Sodium Diarrhea: A Form of Intractable Diarrhea, With a Link to Inflammatory Bowel DiseaseAndreas R Janecke, Peter Heinz-Erian, Thomas MüllerGenes|November 27, 2024
The Recurrent E-Cadherin (CDH1) Mutation c.760G>A Causes Orofacial Clefts but Does Not Predispose to Hereditary CancerLea Gossner, Dietmar Rieder, Thomas Müller, et al.Progress in Molecular Biology and Translational Science|September 3, 2010
Congenital disorders of glycosylation with emphasis on loss of dermatan-4-sulfotransferaseLijuan Zhang, Thomas Müller, Jacques U Baenziger, et al.Clinical Genetics|March 9, 2026
Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial DysplasiaDorothea Stojanovic, Dorota Garczarczyk-Asim, Julia Vodopiutz, et al.Clinical Genetics|October 30, 2024
PERCC1 -Related Congenital EnteropathyLena S Kerle, Pia Karlsland Åkeson, Thomas Müller, et al.Acta Neuropathologica|July 29, 2008
Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 geneKay W Nolte, Andreas R Janecke, Matthias Vorgerd, et al.Wiener Klinische Wochenschrift|September 25, 2010
Lower prevalence of common filaggrin mutations in a community sample of atopic eczema: is disease severity important?Robert Gruber, Andreas R Janecke, Daniela Grabher, et al.Fetal Diagnosis and Therapy|November 27, 2009
Prenatal diagnosis of apert syndrome with cloverleaf skull deformity using ultrasound, fetal magnetic resonance imaging and genetic analysisBenedikt Weber, Anton H Schwabegger, Julia Vodopiutz, et al.JPGN Reports|May 19, 2023
Long-Term Follow-Up of Tufting Enteropathy Caused by EPCAM Mutation p.Asp253Asn and Absent EPCAM ExpressionOğuz Ozler, Andrea Brunner-Véber, Parmis Fatih, et al.European Journal of Pediatrics|July 28, 2009
Refinement of the GINGF3 locus for hereditary gingival fibromatosisMichael Pampel, Sandra Maier, Alfons Kreczy, et al.Pageof 13