- Abort diagnostics
- Array-CGH
- Azoospermia (DAZ)
- Chromosomal aberrations (karyogram, FISH)
- Chromosomal aberrations (Karyogram, FISH)
- chromosome aberration analysis
- Congenital bilateral aplasia of the vas deferens (CBAVD)
- Cri-du-chat syndrome
- Deletion analyses for monogenic diseases
- DiGeorge syndrome (DGS)
- Diplo-Y syndrome (47,XYY syndrome)
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Klinefelter’s syndrome (47,XXY syndrome)
- Mental retardation, impaired development
- Microdeletion 1p36
- Microdeletion 22q13
- Microdeletion syndrome
- Microduplication 22q11.2
- Miller-Dieker syndrome (MDS)
- Muscular dystrophy Duchenne / Becker (MLPA)
- Neurofibromatosis type 1(chromosome 17 FISH analysis, MLPA)
- Patau syndrome (trisomy 13)
- Postnatal Diagnostics
- Prader-Willi syndrome (PWS)
- Prenatal Diagnostics
- Rubinstein-Taybi syndrome (RSTS)
- Shprintzen syndrome (velocardiofacial syndrome (VCFS)
- Smith-Magenis syndrome (SMS)
- Subfertility Analyses (see also Reproductive Genetics)
- Subtelomere
- Subtelomere testing
- Translocation analyses (FISH, M-FISH)
- Triplo-X syndrome (47,XXX syndrome)
- Tuberous sclerosis type 2 (chromosome 16 FISH analysis, MLPA)
- Tumor Cytogenetics (see also Molecular Oncology)
- Ullrich-Turner syndrome (45,X syndrome)
- Williams-Beuren syndrome (WBS)
- Wolf-Hirschhorn syndrome (WHS)
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Accredited according to:
DIN EN ISO /IEC 17025,
DIN EN ISO 15189,
European Fed. of Immunogenetics (EFI)
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