Skip to Content
CALL 773-834-0555
Home
About Us
About Us
Meet the Staff
Photo Gallery
News
Employment Opportunities
Research Collaborators
Fellowship Opportunities
Tests
by Disorder
by Category
by Gene
by Test
Submitting a Sample
Submitting a Sample
Billing Information
Contact
Contact
Suggest A Test
Survey
Employment Opportunities
Employment Opportunities
There are currently no openings in the laboratory. Please check back again soon!
Search
or Choose a Disorder
Allan-Herndon-Dudley syndrome
Alstrom syndrome
Angelman syndrome
Aniridia
asymmetrical polymicrogyria
atypical Rett syndrome
autosomal recessive microcephaly infantile-onset seizures and developmental delay
Autosomal recessive non-syndromic hydrocephalus
autosomal recessive primary microcephaly
Band-like calcification with simplified gyration and polymicrogyria syndrome
Baraitser Winter syndrome
Bernard-Soulier syndrome
bilateral frontoparietal polymicrogyria
brachydactyly type B1
CDPX1
CDPX2
centronuclear myopathy
cerebellar hypoplasia
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease type B
Charcot-Marie-Tooth type 2B1
CHARGE syndrome
CHILD syndrome
CHIME syndrome
Cobblestone Lissencephaly
Complex cortical dysplasia with other brain malformations
Congenital generalized lipodystrophy
congenital variant Rett syndrome
Cornelia de Lange syndrome
Crigler-Najjar syndrome
Dilated cardiomyopathy (DCM)
early infantile epileptic encephalopathy
Emery-Dreifuss Muscular Dystrophy (EDMD)
encephalopathy
familial breast cancer
familial partial lipodystrophy (FLPD) Dunnigan type
Floating Harbor syndrome
Gilbert syndrome
glucose transporter type 1 deficiency syndrome
Goldberg Shprintzen megacolon syndrome
Hallervorden-Spatz syndrome
hearing loss
Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum
Hutchinson-Gilford progeria syndrome (HGPS)
Infantile neuroaxonal dystrophy
Infantile spasms
Intellectual Disability
IPEX syndrome
isolated congenital heart defects
Joubert syndrome
Kabuki syndrome
Limb Girdle Muscular Dystrophies (LGMD)
lissencephaly
Mandibuloacral dysplasia (MAD)
MCSZ
MCT8-specific thyroid hormone cell transporter deficiency
Meckel-Gruber syndrome
Meier-Gorlin syndrome
Menkes disease
Microcephalic Osteodysplastic Primordial Dwarfism type II
microcephaly
Microcephaly-capillary malformation syndrome
MODY
Mowat-Wilson syndrome
myotubular myopathy
NBIA
neonatal diabetes
Neonatal diabetes mellitus
Neurodegeneration with brain iron accumulation type 2 (NBIA2)
Neuroferritinopathy
Oral-Facial-Digital Syndrome Type 1
Pantothenate Kinase-Associated Neurodegeneration
Partial lipodystrophy
PHID
Pitt-Hopkins Syndrome
PKAN
polymicrogyria
pontocerebellar hypoplasia
Prader-Willi syndrome
Rett syndrome
Roberts syndrome
Robinow syndrome
Rubinstein Taybi syndrome
Rubinstein-Taybi syndrome
Russell-Silver syndrome
Schinzel-Giedion syndrome
Seckel Syndrome
Simpson-Golabi-Behmel Syndrome Type 2
Sotos syndrome
Thiamine-responsive megaloblastic anaemia syndrome
Transient neonatal diabetes
UPD14
Warburg Micro syndrome
Weaver syndrome
West syndrome
Wilson disease
Woodhouse-Sakati Syndrome
X-linked Angelman-like syndrome
X-linked dominant chondrodysplasia punctata (CDPX2)
X-linked Female-Limited Epilepsy with Mental Retardation
X-linked Joubert syndrome
X-linked lissencephaly
X-linked mental retardation
X-linked mental retardation and microcephaly with pontine and cerebellar hypoplasia
X-linked myotubular myopathy
X-linked recessive chondrodysplasia punctata (CDPX1)
XLAG
XLAG lissencephaly
XLMR
XLMR with cerebellar hypoplasia
or Choose a Gene
ABCC8
ACSL4
ACTB
ACTG1
AFF2
AGPAT2
AGTR2
AHI1
AKT2
ALMS1
AP1S2
AP4B1
AP4E1
AP4M1
AP4S1
ARFGEF2
ARHGEF6
ARHGEF9
ARID1B
ARL13B
ARSE
ARX
ASPM
ATP6AP2
ATP7A
ATP7B
ATR
ATRX
BCOR
BIN1
BLK
BRCA1
BRCA2
BRWD3
BSCL2
C5orf42
CA8
CASC5
CASK
CASK OPHN1
CAV1
CC2D1A
CC2D2A
CCDC88C
CDC6
CDH15
CDK5RAP2
CDKL5
CDT1
CEL
CENPJ
CEP135
CEP152
CEP290
CEP41
CEP63
CHD7
CIDEC
CISD2
CNTNAP2
CP
CRBN
CREBBP
CUL4B
Cx26
DCAF17
DCX
DLG3
DNM2
DYNC1H1
EBP
EIF2AK3
EP300
ERLIN2
ESCO2
EZH2
FKRP
FKTN
FLNA
FMR1
FOXG1
FOXP1
FOXP3
FTL
FTSJ1
GATA6
GCK
GDI1
GJB2
GLIS3
GLUD1
GP1bP
GPIbβ
GPR56
GRIA3
GRIK2
GRIN2A
GRIN2A MAGI2
GRIN2B
HADH
HCCS
HDAC8
HSD17B10
HUWE1
IER3IP1
IL1RAPL1
INPP5E
INS
INSR
IQSEC2
KCNJ11
KCNQ2
KDM5C
KIA12799
KIAA1279
KIAA12799
KIF7
KIRREL3
KLF11
LARGE
LIS1
LMNA
MAGI2
MAGT1
MAN1B1
MCPH1
MCT8
MECP2
MED12
MED17
MEF2C
MID1
MKS1
MLL2
MPDZ
MSK1
MTM1
NDE1
NEUROD1
NEUROG3
NHS
NIPBL
NKX2.5
NPHP1
NRXN1
NSD1
NSDHL
OCLN
OCRL
OFD1
OPHN1
ORC1
ORC4
ORC6
PAK3
PANK2
PAX4
PAX6
PCDH19
PCNT
PDX1
PHF6
PHF6PHF8
PHF8
PIGL
PLA2G6
PLCB1
PLINI
PLP1
PNKP
POMGNT1
POMT1
POMT2
PPARG
PQBP1
PRPS1
PRSS12
PTCHD1
PTF1A
PTRF
RAB18
RAB39B
RAB3GAP1
RAB3GAP2
RAD21
RAI1
RARS2
RBBP8
RELN
RFX6
RNU4ATAC
ROR2
RPGRIP1L
RPS6KA3
RYR1
SCL2A1
SCN1A
SCN2A
SEPSECS
SETBP1
SHROOM4
SLC12A6
SLC16A2
SLC19A2
SLC25A19
SLC25A22
SLC29A3
SLC2A1
SLC2A2
SLC6A8
SLC9A6
SMADIP1
SMC1A
SMC3
SOBP
SPTAN1
SRCAP
SRPX2
ST3GAL3
STAMBP
STIL
STK9
STXBP1
SYN1
SYNGAP1
SYP
TBC1D4
TCF4
TCTN1
TMEM128
TMEM138
TMEM216
TMEM237
TMEM67
TRAPPC9
TSEN2
TSEN34
TSEN54
TSPAN7
TTC21B
TUB8A
TUBA1A
TUBA8
TUBB2B
TUBB3
TUSC3
UBE2A
UBE3A
UGT1A1
undefined
UPF3B
VLDLR
VRK1
WDR62
WFS1
WNT5A
ZC3H14
ZDHHC9
ZEB2
ZFHX1B
ZFP57
ZMPSTE24
ZNF41
ZNF526
ZNF674
ZNF711
ZNF81
or Choose a Category
Angelman syndrome and Prader-Willi syndrome testing
atypical Rett syndrome testing
Brain Malformation Testing
Centronuclear/myotubular myopathy testing
Chondrodysplasia punctata testing
Cornelia de Lange syndrome testing
Custom mutation analysis
early infantile epileptic encephalopathy testing
exonic deletion/duplication analysis
Intellectual Disability testing
Microcephalic Osteodysplastic Primordial Dwarfism
Microcephaly Testing
Neurodegeneration with brain iron accumulation (NBIA) testing
Next Generation Sequencing
UGT1A1 testing
UPD testing
Home
About Us
About Us
Meet the Staff
Photo Gallery
News
Employment Opportunities
Research Collaborators
Fellowship Opportunities
Tests
by Disorder
by Category
by Gene
by Test
Submitting a Sample
Submitting a Sample
Billing Information
Contact
Contact
Suggest A Test
Survey
Forms
Forms
Test requisition form
Consent Form
List of tests, costs, TAT, CPT codes
In the Spotlight
In the Spotlight
Next Generation Sequencing panels
Cornelia de Lange syndrome
Early Infantile Epileptic Encephalopathy
Microcephaly
Brain Malformation
Kabuki syndrome
Exonic Deletion/Duplication analysis
Newsletter
Newsletter
Join Our Mailing List
Email:
For
Email Marketing
you can trust
