1.
|
MR SpeicherNP CarterThe new cytogenetics:
blurring the boundaries with molecular biologyNat Rev
Genet6782792200510.1038/nrg169216145555
|
2.
|
JP MaciejewskiGJ MuftiWhole genome
scanning as a cytogenetic tool in hematologic
malignanciesBlood112965974200810.1182/blood-2008-02-13043518505780
|
3.
|
JU KangSH KooKC KwonJW ParkJM
KimIdentification of novel candidate target genes, including EPHB3,
MASP1 and SST at 3q26.2–q29 in squamous cell carcinoma of the
lungBMC Cancer9237200919607727
|
4.
|
GS SagooAS ButterworthS SandersonC
Shaw-SmithJP HigginsH BurtonArray CGH in patients with learning
disability (mental retardation) and congenital anomalies: updated
systematic review and meta-analysis of 19 studies and 13,926
subjectsGenet
Med11139146200910.1097/GIM.0b013e318194ee8f19367186
|
5.
|
R HochstenbachE van BinsbergenJ
EngelenArray analysis and karyotyping: workflow consequences based
on a retrospective study of 36,325 patients with idiopathic
developmental delay in the NetherlandsEur J Med
Genet52161169200910.1016/j.ejmg.2009.03.015
|
6.
|
Y ShenKA DiesIA HolmClinical genetic
testing for patients with autism spectrum
disordersPediatrics125727735201010.1542/peds.2009-168420231187
|
7.
|
L EdelmannK HirschhornClinical utility of
array CGH for the detection of chromosomal imbalances associated
with mental retardation and multiple congenital anomaliesAnn NY
Acad Sci1151157166200910.1111/j.1749-6632.2008.03610.x19154522
|
8.
|
SG VorsanovaYB YurovIY IourovHuman
interphase chromosomes: a review of available molecular cytogenetic
technologiesMol Cytogenet31201010.1186/1755-8166-3-120180947
|
9.
|
BA BejjaniLG ShafferApplication of
array-based comparative genomic hybridization to clinical
diagnosticsJ Mol
Diagn8528533200610.2353/jmoldx.2006.06002917065418
|
10.
|
BA BejjaniLG ShafferClinical utility of
contemporary molecular cytogeneticsAnnu Rev Genomics Hum
Genet97186200810.1146/annurev.genom.9.081307.16420718949852
|
11.
|
LG ShafferBA BejjaniMedical applications
of array CGH and the transformation of clinical
cytogeneticsCytogenet Genome
Res115303309200610.1159/00009592817124414
|
12.
|
H TönniesModern molecular cytogenetic
techniques in genetic diagnosticsTrends Mol Med82462502002
|
13.
|
KD LichtenbeltNV KnoersGH
Schuring-BlomFrom karyotyping to array-CGH in prenatal
diagnosisCytogenet Genome
Res135241250201110.1159/00033406522086062
|
14.
|
BA BejjaniR SalekiBC BallifEA RoremK
SundinA TheisenCD KashorkLG ShafferUse of targeted array-based CGH
for the clinical diagnosis of chromosomal imbalance: is less
more?Am J Med Genet A134259267200510.1002/ajmg.a.3062115723295
|
15.
|
JR VermeeschH FieglerN de LeeuwGuidelines
for molecular karyotyping in constitutional genetic diagnosisEur J
Hum Genet1511051114200710.1038/sj.ejhg.520189617637806
|
16.
|
BJ DaveWG SangerRole of cytogenetics and
molecular cytogenetics in the diagnosis of genetic imbalancesSemin
Pediatr Neurol1426200710.1016/j.spen.2006.11.00317331878
|
17.
|
American College of Obstetricians and
GynecologistsACOG Committee Opinion No. 446: array comparative
genomic hybridization in prenatal diagnosisObstet
Gynecol11411611163200910.1097/AOG.0b013e3181c33cad20168129
|
18.
|
BB de VriesR PfundtM LeisinkDiagnostic
genome profiling in mental retardationAm J Hum
Genet77606616200516175506
|
19.
|
P StankiewiczAL BeaudetUse of array CGH in
the evaluation of dysmorphology, malformations, developmental
delay, and idiopathic mental retardationCurr Opin Genet
Dev17182192200710.1016/j.gde.2007.04.00917467974
|
20.
|
LE VissersBB de VriesK OsoegawaArray-based
comparative genomic hybridization for the genomewide detection of
submicroscopic chromosomal abnormalitiesAm J Hum
Genet7312611270200310.1086/37997714628292
|
21.
|
C Shaw-SmithR RedonL RickmanMicroarray
based comparative genomic hybridisation (array-CGH) detects
submicroscopic chromosomal deletions and duplications in patients
with learning disability/mental retardation and dysmorphic
featuresJ Med Genet412412424128200410.1136/jmg.2003.017731
|
22.
|
JR VermeeschC MelotteG FroyenMolecular
karyotyping: array CGH quality criteria for constitutional genetic
diagnosisJ Histochem
Cytochem53413422200510.1369/jhc.4A6436.200515750031
|
23.
|
DT MillerMP AdamS AradhyaConsensus
statement: chromosomal microarray is a first-tier clinical
diagnostic test for individuals with developmental disabilities or
congenital anomaliesAm J Hum
Genet86749764201010.1016/j.ajhg.2010.04.00620466091
|
24.
|
TH BuiA VetroO ZuffardiLG ShafferCurrent
controversies in prenatal diagnosis 3: is conventional chromosome
analysis necessary in the post-array CGH era?Prenat
Diagn31235243201110.1002/pd.272221374637
|
25.
|
BH FaasI van der BurgtAJ
KooperIdentification of clinically significant, submicroscopic
chromosome alterations and UPD in fetuses with ultrasound anomalies
using genome-wide 250k SNP array analysisJ Med
Genet47586594201010.1136/jmg.2009.075853
|
26.
|
SC HillmanS PretloveA CoomarasamyDJ
McMullanEV DavisonER MaherMD KilbyAdditional information from array
comparative genomic hybridization technology over conventional
karyotyping in prenatal diagnosis: a systematic review and
meta-analysisUltrasound Obstet Gynecol37614201110.1002/uog.7754
|