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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,
University of Lausanne, Division of Molecular Pediatrics Bruck Syndrome 2 PLOD2,
University of Lausanne, Division of Molecular Pediatrics Cartilage-Hair Hypoplasia-Anauxetic Dysplasia Spectrum Disorders RMRP,
University of Lausanne, Division of Molecular Pediatrics Chondrodysplasia with Joint Dislocations, GRAPP Type IMPAD1,
University of Lausanne, Division of Molecular Pediatrics CHST3-Related Skeletal Dysplasia CHST3,
University of Lausanne, Division of Molecular Pediatrics Desbuquois Dysplasia CANT1,
University of Lausanne, Division of Molecular Pediatrics DLL3-Related Spondylocostal Dysostosis, Autosomal Recessive DLL3,
University of Lausanne, Division of Molecular Pediatrics Dyssegmental Dysplasia, Silverman-Handmaker Type HSPG2,
University of Lausanne, Division of Molecular Pediatrics Ehlers-Danlos Syndrome, Musculocontractural Type CHST14,
University of Lausanne, Division of Molecular Pediatrics Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly WNT7A,
University of Lausanne, Division of Molecular Pediatrics FKBP10-Related Osteogenesis Imperfecta FKBP10,
University of Lausanne, Division of Molecular Pediatrics HES7-Related Spondylocostal Dysostosis, Autosomal Recessive HES7,
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