Funded by the
National Institutes of Health

Peutz-Jeghers Syndrome | PJS

Select all clinical laboratories
Laboratories offering clinical testing:	Analysis of the entire coding region: Sequence analysis	Sequence analysis of select exons	Linkage analysis	Deletion/duplication analysis	Prenatal diagnosis
Aarhus University Hospital Skejby Molecular Diagnostic Laboratory Aarhus, Denmark Torben Orntoft, MD, DMSci; Else Marie Vestergaard, MD, PhD
Centogene GmbH Institute of Molecular Diagnostics Rostock, Germany Christoph Ehlers
GeneDx Gaithersburg, MD Sherri J Bale, PhD, FACMG; John G Compton, PhD; Anne Maddalena, PhD, FACMG ; Gabriele Richard, MD, FACMG
Liverpool Women's Hospital Mersey Regional Molecular Genetics Laboratory Liverpool, United Kingdom Roger Mountford, BSc, DipRCPath
Medizinisch Genetisches Zentrum Munich, Germany Elke Holinski-Feder, MD
Northwick Park & St Mark's Hospitals Kennedy-Galton Centre, NW Thames Regional Genetics Service Harrow, United Kingdom Stewart Payne, DipRCPath
Sistemas Genomicos Medical Genetics Unit Paterna, Valencia, Spain Javier Garcia-Planells, PhD
The Ohio State University Molecular Pathology Laboratory Columbus, OH Thomas W Prior, PhD, FACMG
University Children's Hospital Labor Molekulargenetik, Abteilung Medizinische Genetik Basel, Switzerland Karl Heinimann, MD, PhD
University of Bonn Institute of Human Genetics Bonn, Germany Markus Noethen, MD
Zentrum fuer Medizinische Genetik Osnabrueck, Germany Anna Gencik, MD; Andrej Gencik, MD, PhD; Heinz Gabriel, PhD

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National Human Genome Research Institute, NIH

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