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Searched: Usher Syndrome Type 1 and Deafness, Autosomal Recessive 23 (DFNB23) via the PCDH15 Gene

Search Results

Usher Syndrome Type 2C and Deafness, Autosomal Recessive 57 (DFNB57) via the PDZD7 Gene

Test Code

Method

Price

11567

Sequencing with CNV PGxome

$990

1466

Sanger Sequencing

$1060
Usher Syndrome Type IJ and Deafness, Autosomal Recessive 48 (DFNB48) via the CIB2 Gene

Test Code

Method

Price

127

Sanger Sequencing

$710

3991

Sequencing with CNV PGxome

$990
Usher Syndrome Type 2 and Deafness, Autosomal Recessive 31 (DFNB31) via the WHRN Gene

Test Code

Method

Price

11807

Sequencing with CNV PGxome

$990

697

Sanger Sequencing

$870
Usher Syndrome Panel

Test Code

Method

Price

10053

Sequencing with CNV PGxome

$990
Usher Syndrome Type 1 via the USH1G Gene

Test Code

Method

Price

649

Sanger Sequencing

$580

8933

Sequencing with CNV PGxome

$990
Hereditary Hearing Loss and Deafness Panel

Test Code

Method

Price

5063

Sequencing with CNV PGxome

$1290
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

Test Code

Method

Price

11651

Sequencing with CNV PGxome

$990

1274

Sanger Sequencing

$780
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1B Gene

Test Code

Method

Price

11649

Sequencing with CNV PGxome

$990

1273

Sanger Sequencing

$870
Deafness, Autosomal Recessive 8 (DFNB8) and Deafness, Autosomal Recessive 10 (DFNB10) via the TMPRSS3 Gene

Test Code

Method

Price

1852

Sanger Sequencing

$870

4271

Sequencing with CNV PGxome

$990
Perrault Syndrome Type 3 and Deafness, Autosomal Recessive 8 (DFNB8) via the CLPP Gene

Test Code

Method

Price

1548

Sanger Sequencing

$650

8691

Sequencing with CNV PGxome

$990
Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1A Gene

Test Code

Method

Price

11647

Sequencing with CNV PGxome

$990

1272

Sanger Sequencing

$780
Inherited Retinal Dystrophies Panel

Test Code

Method

Price

4379

Sequencing with CNV PGxome

$1790
Regeneron Pharmaceuticals Amplify Sponsored Testing

……
Sponsored Hearing Loss Genetic Testing

……
Usher Syndrome Type 2 via the USH2A Gene

Test Code

Method

Price

3059

Sequencing with CNV PG-Select

$990
PGmax^TM - Comprehensive Ocular Disorders Panel

Test Code

Method

Price

12005

Sequencing with CNV PGxome

$1790
Deafness, Autosomal Dominant 36 (DFNA36) and Deafness, Autosomal Recessive 7 (DFNB7) via the TMC1 Gene

Test Code

Method

Price

11751

Sequencing with CNV PGxome

$990

1830

Sanger Sequencing

$1280
Deafness, Autosomal Dominant 22 (DFNA22) and Deafness, Autosomal Recessive 37 (DFNB37) via the MYO6 Gene

Test Code

Method

Price

11499

Sequencing with CNV PGxome

$990

2583

Sanger Sequencing

$1990
Deafness, Autosomal Dominant 12 (DFNA12) and Deafness, Autosomal Recessive 21 (DFNB21) via the TECTA Gene

Test Code

Method

Price

11739

Sequencing with CNV PGxome

$990

2063

Sanger Sequencing

$1560
Deafness, Autosomal Dominant 3A (DFNA3A) and Deafness, Autosomal Recessive 1A (DFNB1A) via the GJB2 Gene

Test Code

Method

Price

7677

Sequencing with CNV PGxome

$990

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Search Results

Usher Syndrome Type 2C and Deafness, Autosomal Recessive 57 (DFNB57) via the PDZD7 Gene

Usher Syndrome Type IJ and Deafness, Autosomal Recessive 48 (DFNB48) via the CIB2 Gene

Usher Syndrome Type 2 and Deafness, Autosomal Recessive 31 (DFNB31) via the WHRN Gene

Usher Syndrome Panel

Usher Syndrome Type 1 via the USH1G Gene

Hereditary Hearing Loss and Deafness Panel

Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1B Gene

Deafness, Autosomal Recessive 8 (DFNB8) and Deafness, Autosomal Recessive 10 (DFNB10) via the TMPRSS3 Gene

Perrault Syndrome Type 3 and Deafness, Autosomal Recessive 8 (DFNB8) via the CLPP Gene

Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1A Gene

Inherited Retinal Dystrophies Panel

Regeneron Pharmaceuticals Amplify Sponsored Testing

Sponsored Hearing Loss Genetic Testing

Usher Syndrome Type 2 via the USH2A Gene

PGmax^TM - Comprehensive Ocular Disorders Panel

Deafness, Autosomal Dominant 36 (DFNA36) and Deafness, Autosomal Recessive 7 (DFNB7) via the TMC1 Gene

Deafness, Autosomal Dominant 22 (DFNA22) and Deafness, Autosomal Recessive 37 (DFNB37) via the MYO6 Gene

Deafness, Autosomal Dominant 12 (DFNA12) and Deafness, Autosomal Recessive 21 (DFNB21) via the TECTA Gene

Deafness, Autosomal Dominant 3A (DFNA3A) and Deafness, Autosomal Recessive 1A (DFNB1A) via the GJB2 Gene