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Products found: 26Search results

Charit Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics

Disorder Genes Test Method Lab Info Product code  
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Blepharophimosis, Ptosis, and Epicanthus Inversus FOXL2, Deletion/duplication analysis
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Blepharophimosis, Ptosis, and Epicanthus Inversus FOXL2, Sequence analysis of the entire coding region
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Camurati-Engelmann Disease TGFB1, Sequence analysis of the entire coding region
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Cleidocranial Dysplasia RUNX2, Deletion/duplication analysis
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Cleidocranial Dysplasia RUNX2, Sequence analysis of the entire coding region
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Congenital Central Hypoventilation Syndrome PHOX2B, Sequence analysis of the entire coding region
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Congenital Central Hypoventilation Syndrome PHOX2B, Targeted mutation analysis
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Congenital Disorders of Glycosylation Multi-Gene Panels
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics DLL3-Related Spondylocostal Dysostosis, Autosomal Recessive DLL3, Sequence analysis of the entire coding region
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Hand-Foot-Genital Syndrome HOXA13, Sequence analysis of the entire coding region
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Hearing Loss/Deafness Multi-Gene Panels
Charité Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics Hyperphosphatasia with Mental Retardation Syndrome 1 PIGV, Sequence analysis of the entire coding region
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