Microdeletion Probes
Description: Alagille syndrome (AGS) is an autosomal dominant disorder characterised by abnormalities of the ...
Description: In 70% of Prader-Willi (PWS) or Angelman Syndrome (AS), a large interstitial deletion of 3-4Mb at ...
Description: The AS UBE3A region probe is optimized to detect copy numbers of the UBE3A gene region at 15q11. ...
Description: CHARGE syndrome is an autosomal dominant disorder that occurs in 1 in 10,000 births. The acronym ...
Description: Cri-Du-Chat syndrome consists of multiple congenital anomalies, mental retardation, microcephaly, ...
Description: The probe is optimized to detect copy numbers at the CTNND2 gene region in the critical region at ...
Description: D5S23, D5S721 probe detects deletions of 5p15.2. The D5S23, D5S721 probe is available alone, or in ...
Description: D5S23, D5S721 probe detects deletions of 5p15.2. The LSI D5S23, D5S721 probe is available alone, or ...
Description: The DGCR2 "N25" region probe covers the marker "N25" (D22S75) and the adjacent region of CLH22 ...
Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...
Description: The 10p14 region probe is optimized to detect copy numbers of the DGS2 at 10p14. The chromosome 10 ...
Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...
Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...
Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...
Description: The GATA4 (8p23) / SE 8 probe is optimized to detect deletions of the GATA4 gene region at 8p23 in ...