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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

Developmental delay with short stature, dysmorphic features, and sparse hair, 616901, Autosomal recessive (Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome) (DPH1 gene) (Sequence Analysis-All Coding Exons) (Postna

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

Developmental delay with short stature, dysmorphic features, and sparse hair, 616901, Autosomal recessive (Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome) (DPH1 gene) (Sequence Analysis-All Coding Exons) (Prenat

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

Craniofacial Panel

Genetic Services Laboratory University of Chicago
United States
3135
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Developmental delay with short stature, dysmorphic facial features, and sparse hair: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Results: 1 to 4 of 4

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