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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Expanded Renal Disease Panel

Invitae
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHRM3 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prune belly syndrome, 100100, Autosomal recessive; PBS (Prune belly syndrome) (CHRM3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Prune belly syndrome, 100100, Autosomal recessive; PBS (Prune belly syndrome) (CHRM3 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Invitae Progressive Renal Disease Panel

Invitae
United States
310195
  • D Deletion/duplication analysis

Prune Belly Syndrome , Sequencing CHRM3 Gene

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

Prune Belly Syndrome (Prenatal Diagnosis) , Sequencing CHRM3 Gene

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

CHRM3 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

Results: 1 to 9 of 9

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