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Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

SNP Microarray Analysis (Chromosomal Microarray)

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
4521
  • D Deletion/duplication analysis
  • H Detection of homozygosity

CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME (Tibial aplasia-ectrodactyly syndrome) (Prenatal) (440)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Split-hand/foot malformation with long bone deficiency 3, 612576, Autosomal dominant (Tibial aplasia-ectrodactyly syndrome) (Prenatal) (440)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Split-hand/foot malformation with long bone deficiency 3, 612576, Autosomal dominant (Tibial aplasia-ectrodactyly syndrome) (440)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Molecular karyotype 180K

Genolife InformaciĆ³n de Vida
Mexico
3416
  • D Deletion/duplication analysis

Results: 1 to 5 of 5

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