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Results: 1 to 17 of 17 (representing 11 labs)

Tests names and labsConditionsGenes and analytesMethods

Cleft lip/palate panel

Centogene AG - the Rare Disease Company
Germany
166
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ankyloblepharon-ectodermal defects-cleft lip/palate

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

TP63. Sequencing of the exons 13 and 14

Instituto de Medicina Genomica
Spain
11
  • E Sequence analysis of select exons

TP63. Sequencing of the exon 3

Instituto de Medicina Genomica
Spain
11
  • E Sequence analysis of select exons

TP63. Complete sequencing

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

TP63 -Related Disorders via the TP63 Gene

PreventionGenetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TP63

Institute for Human Genetics University Clinic Freiburg
Germany
61
  • C Sequence analysis of the entire coding region

Hypospadias Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
7361
  • C Sequence analysis of the entire coding region

TP63 Sequencing

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
61
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ankyloblepharon - ectodermal defects - cleft lip/palate

Bioarray
Spain
11
  • D Deletion/duplication analysis

TP63

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS panel

Fulgent Genetics
United States
370161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ADULT (Acro Dermato Ungual Lacrimal Tooth) Syndrome NGS Panel

Fulgent Genetics
United States
82
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
364163
  • C Sequence analysis of the entire coding region

Limb Malformation: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
12146
  • C Sequence analysis of the entire coding region

Hay-Wells syndrome: TP63 gene screening (exons 13, 14)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • E Sequence analysis of select exons

P63-related disorders

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
31
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Results: 1 to 17 of 17

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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