Disorders

Y Chromosome Detection

Laboratory	Test Method	Prenatal	Carrier *
ARUP Laboratories, Inc., Cytogenetics Laboratory - Salt Lake City, UT, USA	• FISH-metaphase
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA	• FISH-metaphase
bio.logis Center for Human Genetics - Frankfurt, Germany
BioAnalytica-GenoType S.A., Molecular Cytogenetic Research and Applications Lab - Athens, Greece	• Sequence analysis of select exons • Targeted mutation analysis • FISH-metaphase • FISH-interphase • Multicolor FISH (M-FISH)/spectral karotyping(tm) (SKY(tm)) • Mutation scanning of select exons
Boston Children's Hospital, Genetics Diagnostic Laboratory - Waltham, MA, USA
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany	• Targeted mutation analysis
Center for Human Genetics, Inc - Cambridge, MA, USA	• FISH-metaphase • FISH-interphase
CGC Genetics - Porto, Portugal
CGC Genetics USA, Cytogenetics and Molecular Diagnostics Lab - Newark, NJ, USA	• FISH-metaphase
CytoGenX - Stony Brook, NY, USA	• FISH-metaphase • FISH-interphase
Diagnostic Services of Manitoba, Health Sciences Centre site, Molecular Diagnostic Laboratory - Winnipeg, Canada
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel	• Sequence analysis of select exons
Emory University School of Medicine, Emory Molecular Cytogenetics Laboratory - Atlanta, GA, USA	• FISH-metaphase • FISH-interphase
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA
GENNET s.r.o., Laboratory of Molecular Genetics - Prague, Czech Republic
Greenwood Genetic Center, Clinical Cytogenetics Laboratory - Greenwood, SC, USA	• FISH-metaphase • FISH-interphase
Hospital for Sick Children, Molecular Genetics Laboratory - Toronto, Canada	• Targeted mutation analysis
Indiana University School of Medicine, Cytogenetics Laboratory - Indianapolis, IN, USA	• FISH-metaphase • FISH-interphase
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain
Integrated Genetics, Cytogenetics and Biochemistry Laboratory - Santa Fe, NM, USA	• FISH-metaphase • FISH-interphase
LabCorp, Molecular Biology - Research Triangle Park, NC, USA
London Health Sciences Centre, Molecular Diagnostic Laboratory - London, Canada	• Mutation scanning of select exons
Mayo Clinic - Minnesota, Cytogenetics Laboratory - Rochester, MN, USA	• FISH-metaphase • FISH-interphase
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany	• Targeted mutation analysis
Nationwide Children's Hospital, ChildLab Cytogenetics Laboratory - Columbus, OH, USA	• FISH-metaphase • FISH-interphase
Nationwide Children's Hospital, ChildLab Molecular Genetics Laboratory - Columbus, OH, USA	• Targeted mutation analysis
Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center - Portland, OR, USA	• Targeted mutation analysis
Sanford USD Medical Center, Sanford Clinic USD Genetics Laboratory - Sioux Falls, SD, USA	• FISH-metaphase • FISH-interphase
Scott and White Healthcare, Cytogenetics Laboratory - Temple, TX, USA	• FISH-metaphase • FISH-interphase • Multicolor FISH (M-FISH)/spectral karotyping(tm) (SKY(tm))
Seattle Children's Hospital, Cytogenetics - Seattle, WA, USA	• FISH-metaphase • FISH-interphase
Sir Ganga Ram Hospital, Center of Medical Genetics - New Delhi, India	• Targeted mutation analysis • FISH-metaphase • FISH-interphase
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain	• Mutation scanning of select exons
University of Alberta, Molecular Diagnostic Laboratory - Edmonton, Canada
University of California Los Angeles, UCLA Diagnostic Molecular Pathology Laboratory - Los Angeles, CA, USA
University of Colorado Anschutz Medical Campus, Colorado Genetics Laboratory - Denver, CO, USA	• FISH-metaphase • FISH-interphase
University of Oklahoma Health Sciences Center, Genetics Laboratory - Oklahoma City, OK, USA	• Targeted mutation analysis
University of Washington Medical Center, Cytogenetics Laboratory - Seattle, WA, USA	• FISH-metaphase • FISH-interphase • Multicolor FISH (M-FISH)/spectral karotyping(tm) (SKY(tm))

^* 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.