Disorders

Greig Cephalopolysyndactyly Syndrome

Synonym(s): Cephalopolysyndactyly Syndrome, Greig Syndrome

Gene	Locus	Protein
GLI3	7p13	Transcriptional activator GLI3

Laboratory	Test Method	Prenatal	Carrier *
CeGaT GmbH - Tuebingen, Germany
Center for Human Genetics Freiburg, Kohlhase Laboratory - Freiburg, Germany
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany	• Linkage analysis
Centogene AG, Rare Disease Company - Rostock, Germany
Connective Tissue Gene Tests - Allentown, PA, USA
GeneDx - Gaithersburg, MD, USA
Greenwood Genetic Center, Molecular Diagnostic Laboratory - Greenwood, SC, USA
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain
PerkinElmer, Signature Genomic Laboratories - Spokane, WA, USA	• FISH-metaphase
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA	• Linkage analysis

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.