Cerebrospinal Fluid Microscopic Evaluation, Cell Count and Differentiation
Mucopolysaccharidosis type II (Hunter Syndrome)
Chromosome Breakage Study, Chorionic Villi
Bullous pemphigoid
Hemochromatosis
Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
T Cell Receptor Excision Circles (TREC), Molecular Analysis
Hereditary Hearing Loss Gene Panel
Ataxia Telangiectasia Mutated (ATM)
RET/PTC Gene Rearrangement, Molecular
LDS
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