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Results: 21 to 31 of 31

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypomagnesemia NGS Panel

Fulgent Genetics
United States
12123
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bartter Syndrome NGS Panel

Fulgent Genetics
United States
3927
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hypomagnesemia , Panel Massive Sequencing (NGS) 14 Genes

Reference Laboratory Genetics
Spain
1614
  • C Sequence analysis of the entire coding region

Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes

Reference Laboratory Genetics
Spain
2122
  • C Sequence analysis of the entire coding region

HYPOMAGNESEMIA, PRIMARY WITH HYPOCALCURIA (AUTOSOMAL DOMINANT )

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

Renal Hypomagnesemia Type 2 , Sequencing FXYD2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Hypomagnesemia Panel

Blueprint Genetics
Finland
819
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FXYD2 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypomagnesemia 2, renal

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Results: 21 to 31 of 31

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