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Searched: Congenital Cataracts Panel

Search Results

Leukodystrophy and Leukoencephalopathy Panel

Test Code

Method

Price

5495

Sequencing with CNV PGxome

$1490
Congenital Disorders of Glycosylation (CDG) Panel (Types Id, Ie, If, Ig, Ih, Ii)

Test Code

Method

Price

10603

Sequencing with CNV PGxome

$990
Sterol Disorders Panel

Test Code

Method

Price

13319

Sequencing with CNV PGxome

$990
Amelogenesis Imperfecta via the AMELX Gene

Test Code

Method

Price

9161

Sequencing with CNV PGxome

$990

1596

Sanger Sequencing

$440
Retinitis Pigmentosa Panel

Test Code

Method

Price

2699

Sequencing with CNV PGxome

$990
Lipodystrophy Panel

Test Code

Method

Price

12603

Sequencing with CNV PGxome

$990
Congenital Central Hypoventilation Syndrome (CCHS) via the ASCL1 Gene

Test Code

Method

Price

8963

Sequencing with CNV PGxome

$990

777

Sanger Sequencing

$540
Congenital Central Hypoventilation Syndrome (CCHS) via the BMP2 Gene

Test Code

Method

Price

8733

Sequencing with CNV PGxome

$990

2161

Sanger Sequencing

$610
Congenital Generalized Lipodystrophy (CGL) via the CAVIN1 (PTRF) Gene

Test Code

Method

Price

11141

Sequencing with CNV PGxome

$990

4425

Sanger Sequencing

$540
Congenital Hypothyroidism (Thyroid Hormone Resistance) via the THRA Gene

Test Code

Method

Price

11743

Sequencing with CNV PGxome

$990

1585

Sanger Sequencing

$780
Congenital Dyserythropoietic Anemia Type IV via the KLF1 Gene

Test Code

Method

Price

11429

Sequencing with CNV PGxome

$990
Congenital Myopathy (Native American Myopathy) via the STAC3 Gene

Test Code

Method

Price

11717

Sequencing with CNV PGxome

$990

2112

Sanger Sequencing

$780
Lethal Congenital Contracture Syndrome 8 via the ADCY6 Gene

Test Code

Method

Price

13077

Sequencing with CNV PGxome

$990
Lethal Congenital Contracture Syndrome 9 via the ADGRG6 Gene

Test Code

Method

Price

15443

Sequencing with CNV PGxome

$990
Lethal Congenital Contracture Arthrogryposis 11 via the GLDN Gene

Test Code

Method

Price

12657

Sequencing with CNV PGxome

$990
Isolated Nonsyndromic Congenital Heart Defects via the GATA4 Gene

Test Code

Method

Price

9993

Sequencing with CNV PGxome

$990

943

Sanger Sequencing

$650
Congenital Central Hypoventilation Syndrome (CCHS) via the PHOX2A Gene

Test Code

Method

Price

8965

Sequencing with CNV PGxome

$990

1834

Sanger Sequencing

$540
Congenital Disorders of Glycosylation, Type If (CDG If) via the MPDU1 Gene

Test Code

Method

Price

8735

Sequencing with CNV PGxome

$990

538

Sanger Sequencing

$610
Congenital Hypothyroidism and Neonatal Diabetes Mellitus via the GLIS3 Gene

Test Code

Method

Price

11357

Sequencing with CNV PGxome

$990

1586

Sanger Sequencing

$1060
Autosomal Recessive Congenital Ichthyosis (ARCI) via the CYP4F22 Gene

Test Code

Method

Price

8165

Sequencing with CNV PGxome

$990

1163

Sanger Sequencing

$940

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Search Results

Leukodystrophy and Leukoencephalopathy Panel

Congenital Disorders of Glycosylation (CDG) Panel (Types Id, Ie, If, Ig, Ih, Ii)

Sterol Disorders Panel

Amelogenesis Imperfecta via the AMELX Gene

Retinitis Pigmentosa Panel

Lipodystrophy Panel

Congenital Central Hypoventilation Syndrome (CCHS) via the ASCL1 Gene

Congenital Central Hypoventilation Syndrome (CCHS) via the BMP2 Gene

Congenital Generalized Lipodystrophy (CGL) via the CAVIN1 (PTRF) Gene

Congenital Hypothyroidism (Thyroid Hormone Resistance) via the THRA Gene

Congenital Dyserythropoietic Anemia Type IV via the KLF1 Gene

Congenital Myopathy (Native American Myopathy) via the STAC3 Gene

Lethal Congenital Contracture Syndrome 8 via the ADCY6 Gene

Lethal Congenital Contracture Syndrome 9 via the ADGRG6 Gene

Lethal Congenital Contracture Arthrogryposis 11 via the GLDN Gene

Isolated Nonsyndromic Congenital Heart Defects via the GATA4 Gene

Congenital Central Hypoventilation Syndrome (CCHS) via the PHOX2A Gene

Congenital Disorders of Glycosylation, Type If (CDG If) via the MPDU1 Gene

Congenital Hypothyroidism and Neonatal Diabetes Mellitus via the GLIS3 Gene

Autosomal Recessive Congenital Ichthyosis (ARCI) via the CYP4F22 Gene