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Products found: 28Search results

University of Lausanne, Division of Molecular Pediatrics

Disorder Genes Test Method Lab Info Product code  
University of Lausanne, Division of Molecular Pediatrics Absence of Ulna and Fibula with Severe Limb Deficiency WNT7A, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Bruck Syndrome 2 PLOD2, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Cartilage-Hair Hypoplasia-Anauxetic Dysplasia Spectrum Disorders RMRP, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Chondrodysplasia with Joint Dislocations, GRAPP Type IMPAD1, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics CHST3-Related Skeletal Dysplasia CHST3, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Desbuquois Dysplasia CANT1, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics DLL3-Related Spondylocostal Dysostosis, Autosomal Recessive DLL3, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Dyssegmental Dysplasia, Silverman-Handmaker Type HSPG2, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Ehlers-Danlos Syndrome, Musculocontractural Type CHST14, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly WNT7A, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics FKBP10-Related Osteogenesis Imperfecta FKBP10, Sequence analysis of the entire coding region
University of Lausanne, Division of Molecular Pediatrics HES7-Related Spondylocostal Dysostosis, Autosomal Recessive HES7, Sequence analysis of the entire coding region
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