Microdeletion Probes

Description: Alagille syndrome (AGS) is an autosomal dominant disorder characterised by abnormalities of the ...

Cat#: FMDC-01 INQUIRY

Description: In 70% of Prader-Willi (PWS) or Angelman Syndrome (AS), a large interstitial deletion of 3-4Mb at ...

Cat#: FMDC-02 INQUIRY

Description: The AS UBE3A region probe is optimized to detect copy numbers of the UBE3A gene region at 15q11. ...

Cat#: FMDC-03 INQUIRY

Description: CHARGE syndrome is an autosomal dominant disorder that occurs in 1 in 10,000 births. The acronym ...

Cat#: FMDC-04 INQUIRY

Description: Cri-Du-Chat syndrome consists of multiple congenital anomalies, mental retardation, microcephaly, ...

Cat#: FMDC-05 INQUIRY

Description: The probe is optimized to detect copy numbers at the CTNND2 gene region in the critical region at ...

Cat#: FMDC-06 INQUIRY

Description: D5S23, D5S721 probe detects deletions of 5p15.2. The D5S23, D5S721 probe is available alone, or in ...

Cat#: FMDC-07 INQUIRY

Description: D5S23, D5S721 probe detects deletions of 5p15.2. The LSI D5S23, D5S721 probe is available alone, or ...

Cat#: FMDC-08 INQUIRY

Description: The DGCR2 "N25" region probe covers the marker "N25" (D22S75) and the adjacent region of CLH22 ...

Cat#: FMDC-10 INQUIRY

Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...

Cat#: FMDC-11 INQUIRY

Description: The 10p14 region probe is optimized to detect copy numbers of the DGS2 at 10p14. The chromosome 10 ...

Cat#: FMDC-12 INQUIRY

Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...

Cat#: FMDC-13 INQUIRY

Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...

Cat#: FMDC-14 INQUIRY

Description: DiGeorge syndrome, and a variety of congenital malformation syndromes including Velocardiofacial ...

Cat#: FMDC-15 INQUIRY

Description: The GATA4 (8p23) / SE 8 probe is optimized to detect deletions of the GATA4 gene region at 8p23 in ...

Cat#: FMDC-16 INQUIRY

For research use only. Not for any other purpose.