81850-0LOINC 2.82
Chromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics method
Chr 11p15 Methyl + Del+Dup Amn
Definition
- The methylation status and copy numbers of the 11p15 chromosome region can be determined by various methods, including methylation-specific PCR and multiplex ligation-dependent probe amplification (MS-MLPA). This test is performed to detect causes of Beckwith-Wiedemann Syndrome (BWS) and Russell-Silver Syndrome (RSS).
Component
- Chromosome region 11p15 methylation & deletion+duplication
Specimen / system
- Amnio fld
Class
- MOLPATH
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; Amplification; Beckwith Wiedemann Syndrome; BWS; Chr 11p15; Chr 11p15 methylation + deletion+duplication; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; Document; Dp; Finding; Findings; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Methyl + Del+Dup; Molecular genetics; Molecular pathology; MOLPATH; OB; ObGyn; Obstetrics; PCR; Point in time; Random; RSS; Russell-Silver Syndrome
Index terms
- AF
- Amn
- Amn fl
- Amnio
- Amniotic flu
- Amniotic fluid
- Amplification
- Beckwith Wiedemann Syndrome
- BWS
- Chr 11p15
- Chr 11p15 methylation + deletion+duplication
- Chromosom
- Chromosome region 11p15 methylation & deletion+duplication
- Chromosomes
- Cyto loc
- Del
- Del+Dup
- Deletions
- Document
- Dp
- Finding
- Findings
- Genetics
- Gyn
- Gynecology
- Heredity
- Heritable
- Inherited
- Methyl + Del+Dup
- Molecular genetics
- Molecular pathology
- MOLPATH
- OB
- ObGyn
- Obstetrics
- PCR
- Point in time
- Random
- RSS
- Russell-Silver Syndrome