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Results: 1 to 11 of 11

Tests names and labsConditionsGenes and analytesMethods

Baby Genes Targeted Panel

Baby Genes Inc.
United States
8990
  • T Targeted variant analysis

LOR. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Vohwinkel with Ichthyosis Syndrome , Sequencing LOR Gene

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

Keratoderma hereditarium mutilans with ichthyosis

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Ichthyoses and related disorders of cornification Panel

CeGaT GmbH
Germany
4265
  • C Sequence analysis of the entire coding region

LOR

Division Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

LOR

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

LOR

Institute for Human Genetics University Clinic Freiburg
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GJB2/GJB6-Related DFNA3 Nonsyndromic Hearing Loss and Deafness (GJB2/GJB6)

MVZ Dortmund Dr. Eberhard and Partner
Germany
52
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Progressive Symmetric Erythrokeratoderma (sequence analysis of LOR gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2/GJB6)

MVZ Dortmund Dr. Eberhard and Partner
Germany
52
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 11 of 11

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