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Searched: Waardenburg Syndrome Type IIA via the MITF Gene

Search Results

Waardenburg Syndrome Panel

Test Code

Method

Price

10055

Sequencing with CNV PGxome

$990
Waardenburg Syndrome Type IVA via the EDNRB Gene

Test Code

Method

Price

1469

Sanger Sequencing

$680

11003

Sequencing with CNV PGxome

$990
Waardenburg Syndrome Type IVB via the EDN3 Gene

Test Code

Method

Price

1471

Sanger Sequencing

$580

11007

Sequencing with CNV PGxome

$990
Waardenburg Syndrome Type IID via the SNAI2 Gene

Test Code

Method

Price

1539

Sanger Sequencing

$540

9051

Sequencing with CNV PGxome

$990
Oculocutaneous Albinism and Hypopigmentation Panel

Test Code

Method

Price

10313

Sequencing with CNV PGxome

$990
Waardenburg Syndrome Types IIE and IVC via the SOX10 Gene

Test Code

Method

Price

1472

Sanger Sequencing

$680

8615

Sequencing with CNV PGxome

$990
Waardenburg Syndrome Types I and III via the PAX3 Gene

Test Code

Method

Price

1468

Sanger Sequencing

$680

8613

Sequencing with CNV PGxome

$990
Hereditary Hearing Loss and Deafness Panel

Test Code

Method

Price

5063

Sequencing with CNV PGxome

$1290
Deafness, Autosomal Dominant 69 (DFNA69), and Familial Progressive Hyperpigmentation with or without Hypopigmentation via the KITLG Gene

Test Code

Method

Price

4433

Sanger Sequencing

$750

5043

Sequencing with CNV PGxome

$990
Microphthalmia/Anophthalmia/Coloboma Panel

Test Code

Method

Price

10333

Sequencing with CNV PGxome

$990
Regeneron Pharmaceuticals Amplify Sponsored Testing

…This comprehensive panel consists of genes that have been associated with all types of HHLD. Importantly, both syndromic and nonsyndromic HL genes are included in this panel due to the variable or mild features associated with some syndromic…
Sponsored Hearing Loss Genetic Testing

…types of syndromic hearing loss are Usher, Waardenburg, and Pendred syndromes (Koffler et al. 2015. PubMed ID: 26443487). Other less common syndromic causes of hearing loss are also included in this panel (Perrault, Treacher Collins…
Common Hereditary Cancer Screening Panel

Test Code

Method

Price

15723

Sequencing with CNV PG-Select

$990
Comprehensive Pediatric Solid Tumor Panel

Test Code

Method

Price

7973

Sequencing with CNV PG-Select

$1290
PGmax^TM - Comprehensive Ocular Disorders Panel

Test Code

Method

Price

12005

Sequencing with CNV PGxome

$1790
All

…the SNAI2 Gene Test Code Method Price 1539 Sanger Sequencing $540 9051 Sequencing with CNV PGxome $990 Waardenburg Syndrome Type IVA via the EDNRB Gene Test Code Method Price 1469 Sanger Sequencing $680 11003 Sequencing with CNV PGxome $990…
Overgrowth and Macrocephaly Syndromes Panel

Test Code

Method

Price

3449

Sequencing with CNV PGxome

$1290
Anterior Segment Dysgenesis Disorders Panel

Test Code

Method

Price

12003

Sequencing with CNV PGxome

$1290
Renal Cancer Panel

Test Code

Method

Price

1331

Sequencing with CNV PG-Select

$990
MYH9-Related Disorders via the MYH9 Gene

Test Code

Method

Price

11491

Sequencing with CNV PGxome

$990

438

Sanger Sequencing

$1750

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Search Results

Waardenburg Syndrome Panel

Waardenburg Syndrome Type IVA via the EDNRB Gene

Waardenburg Syndrome Type IVB via the EDN3 Gene

Waardenburg Syndrome Type IID via the SNAI2 Gene

Oculocutaneous Albinism and Hypopigmentation Panel

Waardenburg Syndrome Types IIE and IVC via the SOX10 Gene

Waardenburg Syndrome Types I and III via the PAX3 Gene

Hereditary Hearing Loss and Deafness Panel

Deafness, Autosomal Dominant 69 (DFNA69), and Familial Progressive Hyperpigmentation with or without Hypopigmentation via the KITLG Gene

Microphthalmia/Anophthalmia/Coloboma Panel

Regeneron Pharmaceuticals Amplify Sponsored Testing

Sponsored Hearing Loss Genetic Testing

Common Hereditary Cancer Screening Panel

Comprehensive Pediatric Solid Tumor Panel

PGmax^TM - Comprehensive Ocular Disorders Panel

All

Overgrowth and Macrocephaly Syndromes Panel

Anterior Segment Dysgenesis Disorders Panel

Renal Cancer Panel

MYH9-Related Disorders via the MYH9 Gene