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Searched: Chromosome 5q14.3 Deletion Syndrome via the MEF2C Gene

Search Results

Y Chromosome Deletion Analysis

Test Code

Method

Price

3740

Targeted Deletion

$350
Rett Syndrome, Angelman Syndrome and Variant Syndromes Panel

Test Code

Method

Price

3257

Sequencing with CNV PGxome

$990
Hermansky-Pudlak Syndrome via the HPS3 Gene, Exon 1 Deletion

Test Code

Method

Price

759

Targeted Deletion

$350
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

$990
Top 99 Genetic Causes of Developmental Delay Panel

Test Code

Method

Price

12675

Sequencing with CNV PGxome

$990
Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A 1q21.1 Deletion

Test Code

Method

Price

1718

CMA

$750
Wagner Syndrome via the VCAN Gene

Test Code

Method

Price

11791

Sequencing with CNV PGxome

$990

523

Sanger Sequencing

$1840
Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A Gene - Sequencing and 1q21.1 Deletion

Test Code

Method

Price

1719

CMA & Sanger Sequencing

$1190
Manitoba Oculotrichoanal Syndrome (MOTA) via the FREM1 Exon 8-23 Deletion

Test Code

Method

Price

3782

Targeted Deletion

$350
Early Infantile Epileptic Encephalopathy Panel

Test Code

Method

Price

10429

Sequencing with CNV PGxome

$1290
Cystinosis via the CTNS Gene, 57-kb Deletion

Test Code

Method

Price

1636

Targeted Deletion

$350
Nemaline Myopathy via the NEB Exon 55 Deletion

Test Code

Method

Price

356

Targeted Deletion

$350
Tay-Sachs Disease via the French Canadian Deletion in the HEXA Gene

Test Code

Method

Price

1450

Targeted Deletion

$350
Cerebral Cavernous Malformations via the CCM2 Gene, Exons 2-10 Deletion

Test Code

Method

Price

124

Targeted Deletion

$350
Paroxysmal Paralytic Rhabdomyolysis via the LPIN1 Gene, Exons 18-19 Deletion

Test Code

Method

Price

319

Targeted Deletion

$350
Del Dup and Array

……
Rapid Prenatal Chromosomal Microarray via the aCGH and SNP - Prenatal Test #3780

Test Code

Method

Price

3780

CMA

$1390
Rapid Chromosomal Microarray via aCGH and SNP Test #12684

Test Code

Method

Price

12684

CMA

$1250
Whole-Genome Chromosomal Microarray (CMA-ISCA) via the aCGH and SNP Test #2000

Test Code

Method

Price

2000

CMA

$990
Oculocutaneous Albinism Type 2 (OCAII) via the OCA2 Known Intragenic Gross Deletion

Test Code

Method

Price

3738

Targeted Deletion

$350

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Search Results

Y Chromosome Deletion Analysis

Rett Syndrome, Angelman Syndrome and Variant Syndromes Panel

Hermansky-Pudlak Syndrome via the HPS3 Gene, Exon 1 Deletion

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

Top 99 Genetic Causes of Developmental Delay Panel

Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A 1q21.1 Deletion

Wagner Syndrome via the VCAN Gene

Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A Gene - Sequencing and 1q21.1 Deletion

Manitoba Oculotrichoanal Syndrome (MOTA) via the FREM1 Exon 8-23 Deletion

Early Infantile Epileptic Encephalopathy Panel

Cystinosis via the CTNS Gene, 57-kb Deletion

Nemaline Myopathy via the NEB Exon 55 Deletion

Tay-Sachs Disease via the French Canadian Deletion in the HEXA Gene

Cerebral Cavernous Malformations via the CCM2 Gene, Exons 2-10 Deletion

Paroxysmal Paralytic Rhabdomyolysis via the LPIN1 Gene, Exons 18-19 Deletion

Del Dup and Array

Rapid Prenatal Chromosomal Microarray via the aCGH and SNP - Prenatal Test #3780

Rapid Chromosomal Microarray via aCGH and SNP Test #12684

Whole-Genome Chromosomal Microarray (CMA-ISCA) via the aCGH and SNP Test #2000

Oculocutaneous Albinism Type 2 (OCAII) via the OCA2 Known Intragenic Gross Deletion