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  • DNA in a shopping cart Leukoencephalopathy with Vanishing White Matter and Ovarioleukodystrophy via the EIF2B2 Gene
    Test Code
    Method
    Price
    612
    Sanger Sequencing
    $610
    8763
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Junctional Epidermolysis Bullosa via the LAMB3 Gene
    Test Code
    Method
    Price
    7723
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Lethal Contracture Syndrome 7 via the CNTNAP1 Gene
    Test Code
    Method
    Price
    15485
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hirschsprung Disease (Non-syndromic) Panel
    Test Code
    Method
    Price
    10225
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Holoprosencephaly-2 (Autosomal Dominant, Nonsyndromic) via the SIX3 Gene
    Test Code
    Method
    Price
    583
    Sanger Sequencing
    $560
    8937
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hirschsprung Disease 3 (HSCR3) via the GDNF Gene
    Test Code
    Method
    Price
    1566
    Sanger Sequencing
    $540
    8995
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hypogonadotropic Hypogonadism/Kallmann Syndrome via the WDR11 Gene
    Test Code
    Method
    Price
    12649
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Homocystinuria, cblE Type, via the MTRR Gene
    Test Code
    Method
    Price
    888
    Sanger Sequencing
    $1060
    11843
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Heterotaxy and Conotruncal Heart Defects via the GDF1 Gene
    Test Code
    Method
    Price
    8875
    Sequencing with CNV PGxome
    $890
    937
    Sanger Sequencing
    $580
  • DNA in a shopping cart Holoprosencephaly-9 (Autosomal Dominant, Nonsyndromic) via the GLI2 Gene
    Test Code
    Method
    Price
    11355
    Sequencing with CNV PGxome
    $890
    586
    Sanger Sequencing
    $1080
  • DNA in a shopping cart Histiocytosis-Lymphadenopathy Plus Syndrome via the SLC29A3 Gene
    Test Code
    Method
    Price
    11001
    Sequencing with CNV PGxome
    $890
    5319
    Sanger Sequencing
    $750
  • DNA in a shopping cart Metachromatic Leukodystrophy via the PSAP Gene
    Test Code
    Method
    Price
    7169
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Lujan Syndrome, FG Syndrome Type 1 and Ohdo Syndrome via the MED12 Gene
    Test Code
    Method
    Price
    7991
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Klippel-Feil Syndrome Panel
    Test Code
    Method
    Price
    12621
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Leber Congenital Amaurosis Panel
    Test Code
    Method
    Price
    4313
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Lissencephaly Panel
    Test Code
    Method
    Price
    5047
    Sequencing with CNV PGxome
    $1070
  • DNA in a shopping cart Merosin-Deficient Congenital Muscular Dystrophy (MDC1A) via the LAMA2 Gene, Exon 55
    Test Code
    Method
    Price
    245
    Sanger Sequencing
    $250
  • DNA in a shopping cart Loeys-Dietz Syndrome via the SMAD3 Gene
    Test Code
    Method
    Price
    7319
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Klippel-Feil Syndrome via the MEOX1 Gene
    Test Code
    Method
    Price
    838
    Sanger Sequencing
    $610
    8759
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Methylmalonate Semialdehyde Dehydrogenase Deficiency via the ALDH6A1 Gene
    Test Code
    Method
    Price
    11823
    Sequencing with CNV PGxome
    $890
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