Funded by the
National Institutes of Health

Sulfate Transporter-Related Osteochondrodysplasia
Includes: Achondrogenesis Type 1B | Atelosteogenesis Type II | Diastrophic Dysplasia | Multiple Epiphyseal Dysplasia, Recessive

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Targeted mutation analysis	Enzyme assay	Prenatal diagnosis	Carrier testing
Connective Tissue Gene Tests Allentown, PA James C Hyland, MD, PhD; Leena M Ala-Kokko, MD, PhD
HUSLAB Laboratory of Molecular Genetics Helsinki, Finland Aarno Palotie, MD, PhD; Arto K Orpana, PhD
University of Lausanne Division of Molecular Pediatrics Lausanne, Switzerland Luisa Bonafe, MD, PhD
Zentrum fuer Medizinische Genetik Osnabrueck, Germany Anna Gencik, MD; Andrej Gencik, MD, PhD; Heinz Gabriel, PhD

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National Library of Medicine, NIH
National Human Genome Research Institute, NIH

Sponsoring Institution
University of Washington
Seattle, Washington