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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pontocerebellar hypoplasia, type 3, 608027, Autosomal recessive; PCH3 (Pontocerebellar hypoplasia type 3) (PCLO 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

Pontocerebellar hypoplasia, type 3, 608027, Autosomal recessive; PCH3 (Pontocerebellar hypoplasia type 3) (PCLO 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

Invitae Epilepsy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
466297
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pontocerebellar hypoplasia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2018
  • C Sequence analysis of the entire coding region

Microcephaly and Pontocerebellar Hypoplasia Panel

CeGaT GmbH
Germany
3836
  • C Sequence analysis of the entire coding region

Microcephaly and Pontocerebellar Hypoplasia Panel

CeGaT GmbH
Germany
3836
  • C Sequence analysis of the entire coding region

Pontocerebellar Hypoplasia Type 3

Gleeson Lab University of California San Diego - Department of Neuroscience
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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