Targeted Gene Mutation Panel, Solid Organ Neoplasm (PancreaSeq)
Complement Component CH50
Complement Component C1q
Secobarbital, Urine
Creatinine Random, Urine
CDKN1C Gene Mutation Analysis
Complement Component C4
Oligoclonal Bands, Serum
Atypical Pneumonia DNA Panel, Bronchial Wash/Lavage
Kidney Stone Analysis
LDS
Sign up
Log in
LDS
/
Medical Tests
/
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Medical Test
References
Access to
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
is restricted.
Sign up now
Loading...