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Searched: Galloway Mowat Syndrome (GAMOS) via the GON7��Gene

Search Results

Roberts Syndrome via the ESCO2 Gene

Test Code

Method

Price

11301

Sequencing with CNV PGxome

$890

836

Sanger Sequencing

$830
Temtamy Syndrome via the C12orf57 Gene

Test Code

Method

Price

13049

Sequencing with CNV PGxome

$890
TARP Syndrome via the RBM10 Gene

Test Code

Method

Price

2475

Sanger Sequencing

$1280

8029

Sequencing with CNV PGxome

$890
Tenorio Syndrome via the RNF125 Gene

Test Code

Method

Price

3789

Sanger Sequencing

$710

8501

Sequencing with CNV PGxome

$890
All

……
Oculocerebrorenal Syndrome of Lowe (Lowe syndrome) and Dent Disease - 2 via the OCRL Gene

Test Code

Method

Price

11539

Sequencing with CNV PGxome

$890

1640

Sanger Sequencing

$1280
Medulloblastoma and Nevoid Basal Cell Carcinoma Syndrome/Gorlin Syndrome via the SUFU Gene

Test Code

Method

Price

8303

Sequencing with CNV PG-Select

$640
Duane-Radial Ray Syndrome and Acro-Renal-Ocular Syndrome via the SALL4 Gene

Test Code

Method

Price

832

Sanger Sequencing

$730

8459

Sequencing with CNV PGxome

$890
Aicardi-Goutières Syndrome 7 and Singleton-Merton Syndrome 1 via the IFIH1 Gene

Test Code

Method

Price

11383

Sequencing with CNV PGxome

$890

2918

Sanger Sequencing

$1190
X-linked Lenz Microphthalmia Syndrome and Lethal Ogden Syndrome via the NAA10 Gene

Test Code

Method

Price

2006

Sanger Sequencing

$680

8617

Sequencing with CNV PGxome

$890
Differences of Sex Development (DSD) and Infertility Panel

Test Code

Method

Price

2669

Sequencing with CNV PGxome

$1490
Early Infantile Epileptic Encephalopathy Panel

Test Code

Method

Price

10429

Sequencing with CNV PGxome

$1240
Comprehensive Congenital Heart Disease Panel

Test Code

Method

Price

13008

Sequencing with CNV PGxome

$1490
Phelan-Mcdermid Syndrome, 22q13 Deletion Syndrome, or Autism Spectrum Disorder via the SHANK3 Gene

Test Code

Method

Price

1524

Sanger Sequencing

$1590

9841

Sequencing with CNV PGxome

$890
Amelogenesis Imperfecta with Gingival Hyperplasia Syndrome and Amelogenesis Imperfecta with Renal Syndrome via the FAM20A Gene

Test Code

Method

Price

11319

Sequencing with CNV PGxome

$890

1602

Sanger Sequencing

$840
Seckel Syndrome, Primary Microcephaly and Familial Cutaneous Telangiectasia and Cancer Syndrome via the ATR Gene

Test Code

Method

Price

7979

Sequencing with CNV PGxome

$890

1291

Sanger Sequencing

$2450
Non-Immune Hydrops Fetalis Panel

Test Code

Method

Price

12661

Sequencing with CNV PGxome

$1240
Nail-Patella Syndrome via the LMX1B Gene

Test Code

Method

Price

1458

Sanger Sequencing

$680

8581

Sequencing with CNV PGxome

$890
Noonan-Like Syndrome via the RRAS Gene

Test Code

Method

Price

10641

Sequencing with CNV PG-Select

$640
Li-Fraumeni Syndrome via the TP53 Gene

Test Code

Method

Price

7521

Sequencing with CNV PG-Select

$540

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Search Results

Roberts Syndrome via the ESCO2 Gene

Temtamy Syndrome via the C12orf57 Gene

TARP Syndrome via the RBM10 Gene

Tenorio Syndrome via the RNF125 Gene

All

Oculocerebrorenal Syndrome of Lowe (Lowe syndrome) and Dent Disease - 2 via the OCRL Gene

Medulloblastoma and Nevoid Basal Cell Carcinoma Syndrome/Gorlin Syndrome via the SUFU Gene

Duane-Radial Ray Syndrome and Acro-Renal-Ocular Syndrome via the SALL4 Gene

Aicardi-Goutières Syndrome 7 and Singleton-Merton Syndrome 1 via the IFIH1 Gene

X-linked Lenz Microphthalmia Syndrome and Lethal Ogden Syndrome via the NAA10 Gene

Differences of Sex Development (DSD) and Infertility Panel

Early Infantile Epileptic Encephalopathy Panel

Comprehensive Congenital Heart Disease Panel

Phelan-Mcdermid Syndrome, 22q13 Deletion Syndrome, or Autism Spectrum Disorder via the SHANK3 Gene

Amelogenesis Imperfecta with Gingival Hyperplasia Syndrome and Amelogenesis Imperfecta with Renal Syndrome via the FAM20A Gene

Seckel Syndrome, Primary Microcephaly and Familial Cutaneous Telangiectasia and Cancer Syndrome via the ATR Gene

Non-Immune Hydrops Fetalis Panel

Nail-Patella Syndrome via the LMX1B Gene

Noonan-Like Syndrome via the RRAS Gene

Li-Fraumeni Syndrome via the TP53 Gene