polysomy (Also polysomies) : Related Words Words similar in meaning to polysomy

polysomy«
chromosome«
congenital disorder«
trisomy«
congenital defect«
tetrasomy«
congenital anomaly«
karyotype«
congenital abnormality«
extra chromosome«
birth defect«
x polysomy«
polysomy x«
chromosome polysomy«
x chromosome«
nondisjunction«
fluorescence«
aneuploidy«
situ hybridization«
gene«
polysomic inheritance«
metafemales«
centric fusion«
sperm development«
chromosomal aneuploidy«
meiosis«
tetrasomy 9p«
male grasshopper«
tetrasomy 18p«
cell«
terc«
karyotyping«
lymphosarcoma«
fetal cell«
giemsa«
restriction fragment length polymorphism«
isozymes«
extra copy«
amniocentesis«
polyploidy«
centromere«
copy«
chromosomal abnormality«
egfr«
sex chromosome«
incidence«
diploid«
squamous cell carcinoma«
aml«
disjunction«
dna«
down syndrome«
rearrangement«
egg«
mechanism«
abnormality«
prostate cancer«
yeast rna1 gene«
xxy. x chromosome polysomy«
villous sampling«
unnecessary cancer treatment«
unbalanced chromosome«
tumerogenesis«
translocation mutation(a chromosome abnormality«
suffix -ploidy«
submicroscopic chromosomal abnormality«
specie gryllotalpa gryllotalpa«
situ hybridization test«
roderick r. mcinnes«
prenatal diagnostic tests«
prenatal diagnosis phase«
polysomy type«
polysomy increase«
polysomic mosaic«
ornithogalum umbellatum l.«
onset autosomal disorder«
multivalents«
most eukaryotic specie«
mole cricket chromosome«
maternal blood sampling«
margaret w. thompson«
karyotype rearrangement«
karyotype image«
kallionemi«
interchange heterozygote«
indrajit nanda«
human telomerase rna component«
human polysomy x«
human lymphocyte culture«
human chromosome 8q«
hexasomy«
heterochromic polysomy«
heterochromatic polysomy«
her2 testing result«
her2 gene copy«
grasshopper«
germ line polysomy«
frequent genetic disorder«
flor strain«
few fungi«
fetal karyotype«
fetal chromosome status«
ethanol oxidative utilization«
entire karyotype«
eeva therman«
e chromosome abnormality«
cultivar r570«
conventional cytogenic technique«
common karyotypic«
common autosomies«
chromosome today«
chromosome heteromorphisms«
chorthippus binotatus«
centromeric misdivision«
canine osteoid chondrosarcoma«
canine leukemia«
adh3 locus«
ada hamosh«
abnormal brain mri«
conjunction«
linkage«
thompson genetics«
tetrasomic inheritance«
suffix -somy«
successive nondisjunction«
mother increase«
lisa g. shaffer«
leu2 sequence«
homologous partner«
her2/neu gene«
chromosome a9«
atractomorpha similis«
aneuploid karyotype«
adh2«
fish«
segregation«
future generation«
somatic abnormality«
orlando j.«
month survival rate«
microarray technique«
hypodiploidy«
hemangiopericytomas«
grant r. sutherland«
extra e«
autopolyploids«
several cell«
hyperdiploidy«
egfr expression«
developmental retardation«
chromosomal microarray analysis«
canine chromosome«
spectral karyotyping«
huntington f. willard«
cytometry«
canine tumor«
type«
yeast specie saccharomyces cerevisiae«
specific cell population«
nonhomologous chromosome«
fish analysis«
aneuploids«
ultrasound finding«
diagnostic tools«
chromosomal duplication«
physical malformation«
conventional cytogenetics«
normal sperm«
renal anomaly«
marker chromosome«
cytogenetic technique«
b chromosome«
array comparative genomic hybridization«
flow cytometers«
ventriculomegaly«
southern blot analysis«
snp array«
paspalum dilatatum«
newborn male«
secondary disease«
pulsed field gel electrophoresis«
fungi«
isochromosome«
thyroid tumor«
abnormal chromosome«
normal chromosome«
extra x chromosome«
biological aging«
plant«
growth restriction«
germ line cell«
male«
unique light«
individual chromosome«
organism«
prenatal ultrasound«
huntingtin«
fluorescent label«
myeloproliferative disorder«
exact multiple«
comparative genomic hybridization«
immunocytochemistry«
uc san francisco«
placental tissue«
single chromosome«
polyploid«
breast carcinoma«
microarray analysis«
set«
mole cricket«
prenatal«
euphrasia«
chromosome abnormality«
tumor development«
mosaicism«
chorionic villus sampling«
klinefelter syndrome«
heterochromatin«
alcohol dehydrogenase«
diagnostic technique«
growth retardation«
female parent«
kluwer academic«
protein«
epidermal growth factor receptor«
homologous chromosome«
clinical evaluation«
microarray«
independent event«
liliaceae«
chemotherapeutic agent«
brassica«
sky«
mating system«
myelodysplastic syndrome«
genetic counseling«
flow cytometry«
dna fragment«
living environment«
trypsin«
amniotic fluid«
restriction enzyme«
cancer diagnosis«
human chromosome«
genetic condition«
acute myeloid leukemia«
natural population«
strabismus«
clinical diagnosis«
patient«
gene responsible«
dark band«
cleft lip«
gene product«
cytology«
short arm«
developmental delay«
scoliosis«
fluorescent«
overexpression«
rare condition«
disease«
robert l.«
specific site«
diagnostic tool«
risk«
schmid«
oxford up«
polymerase chain reaction«
medicine«
trisomy 21«
tongue tie«
syndactyly«
syndactylism«
spinocerebellar disorder«
spina bifida«
schistorrhachis«
scaphocephaly«
rachischisis«
pseudohermaphroditism«
polydactyly«
plagiocephaly«
oxycephaly«
myelomeningocele«
mongolism«
mongolianism«
meromelia«
meningocele«
macroglossia«
hyperdactyly«
hermaphroditism«
hermaphrodism«
harelip«
epispadias«
encephalocele«
congenital heart defect«
colour vision deficiency«
colour blindness«
color vision deficiency«
color blindness«
clinodactyly«
clinocephaly«
clinocephalism«
cleft palate«
cheiloschisis«
ankyloglossia«
anencephaly«
anencephalia«
ametria«
amelia«
albinism«
acrocephaly«
ablepharia«
tetralogy of Fallot«
septal defect«
seal limbs«
phocomelia«
monochromia«
monochromatism«
monochromatic vision«
monochromasy«
monochromacy«
dichromia«
dichromatopsia«
dichromatism«
dichromasy«
dichromacy«
adactyly«
adactylism«
adactylia«
49,xxxxy. polysomy y«
18p formation«
48,xxxy«
18th chromosome«
47,xyy«
21st chromosome«
Down's syndrome«
Down syndrome«
Fallot's tetralogy«
Fallot's syndrome«

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