trisomy

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(Click for frequent words.) 69 Trisomy 66 neural tube defect 64 anencephaly 64 chromosomal abnormalities 64 chromosomal disorder 63 chromosomal defect 62 fetal aneuploidy 62 chromosomal abnormality 62 aneuploidy 61 congenital anomalies 61 diagnosed prenatally 60 TTTS 60 hydrops 60 pyloric stenosis 59 chromosome abnormality 59 prenatally diagnosed 59 genetic abnormalities 59 IgA deficiency 59 preterm deliveries 59 Patau syndrome 59 chromosomal disorders 58 genetic abnormality 58 Down syndrome 58 aneuploidies 58 bronchopulmonary dysplasia 58 twin transfusion 58 gastroschisis 58 chromosome abnormalities 58 myelomeningocele 57 genetic syndromes 57 Apert syndrome 57 LQTS 57 IUGR 57 Klinefelter syndrome 57 holoprosencephaly 57 DiGeorge syndrome 57 Joubert syndrome 57 pre eclamptic 57 Beckwith Wiedemann syndrome 57 breast carcinomas 57 polyhydramnios 57 inherited mutations 57 diaphragmatic hernia 57 RhD 57 mosaicism 57 karyotype 57 dizygotic twins 56 HbF 56 FMR1 56 neurodevelopmental impairment 56 fetal malformations 56 IVF ICSI 56 Hurler syndrome 56 lymph node metastasis 56 congenital diaphragmatic hernia 56 Rh incompatibility 56 congenital abnormalities 56 autosomal dominant 56 chromosomal defects 56 fetal chromosomal abnormalities 56 hemolytic disease 56 heterozygous 56 congenital disorder 56 autosomal recessive 55 transfusion syndrome 55 Dravet syndrome 55 NF1 55 dizygotic 55 chorionic villus sampling 55 MCADD 55 prenatal diagnosis 55 CMV infection 55 congenital anomaly 55 weeks gestation 55 teratoma 55 thrombophilia 55 FMR1 gene 55 congenital malformations 55 CHDs 55 persistent pulmonary hypertension 55 placental abruption 55 autosomal dominant disorder 55 HLHS 55 cryptorchidism 55 ependymoma 55 BRCA mutations 55 hamartomas 54 intraventricular hemorrhage 54 congenital disorders 54 asymptomatic hypothyroidism 54 Ebstein anomaly 54 Hirschsprung disease 54 missense mutations 54 singleton pregnancy 54 advanced adenoma 54 aneuploid 54 abnormalities 54 varicocele 54 hypoplasia 54 Wilms tumor 54 DiGeorge Syndrome 54 ASDs 54 hydronephrosis 54 recurrent miscarriage 54 fetal chromosomal 54 pulmonary hypoplasia 54 Folate supplementation 54 autosomal 54 Fanconi anemia 54 aneuploidy screening 54 sporadic ALS 54 adenomatous polyps 54 intra uterine 54 atresia 54 #q#.# [001] 54 leiomyomas 54 abnormal chromosomes 54 lissencephaly 54 ectopic 54 congenital hypothyroidism 54 hypoplastic left 54 amniocentesis 54 tricuspid atresia 54 mtDNA mutations 54 monozygotic twins 54 hyperbilirubinemia 53 chromosomal anomaly 53 monozygotic 53 Angelman syndrome 53 SNHL 53 Retinopathy 53 singleton pregnancies 53 pulmonary atresia 53 ovarian tumors 53 ADPKD 53 microalbuminuria 53 Amniocentesis 53 neurofibromas 53 postnatally 53 malformations 53 thyroglobulin 53 achondroplasia 53 GISTs 53 ambiguous genitalia 53 adnexal mass 53 preterm delivery 53 beta thalassemia 53 BRCA2 mutation carriers 53 adenoma 53 RPE# 53 mutation 53 mutant alleles 53 Langerhans cell histiocytosis 53 congenital adrenal hyperplasia CAH 53 choriocarcinoma 53 VUR 53 blastocyst 53 ventricular septal defect 53 microsatellite instability 53 medulloblastoma 53 multiple gestations 53 molar pregnancy 53 fetu 53 spontaneous preterm birth 53 severe hyperbilirubinemia 53 born preterm 53 uterus didelphys 53 familial ALS 53 primary ovarian insufficiency 53 inhibin 53 penetrance 53 biliary atresia 53 BRCA1 mutations 53 malformation 53 fetal abnormalities 53 toxoplasmosis 53 ectopic pregnancies 53 prepubertal 53 advanced neoplasia 53 sirenomelia 53 RhD negative 53 utero 52 amniotic fluid embolism 52 sonographic findings 52 craniosynostosis 52 polycystic ovaries 52 homozygosity 52 MCAD deficiency 52 hyperplastic 52 placental malaria 52 chromosomal anomalies 52 neural tube defects 52 atypical hyperplasia 52 Heterozygous 52 rare chromosomal disorder 52 polycystic ovary syndrome PCOS 52 atypia 52 karyotypes 52 BRCA1 52 alleles 52 truncus arteriosus 52 subclinical 52 leiomyoma 52 fertilized egg splits 52 necrotizing enterocolitis 52 galactosemia 52 Tay Sachs disease 52 pre eclampsia 52 Spina bifida 52 polydactyly 52 subclinical hypothyroidism 52 endometrial cancers 52 congenital malformation 52 TP# mutations 52 homozygotes 52 preeclampsia 52 heterotaxy 52 dysplasia 52 spontaneous mutation 52 febrile seizures 52 NF2 52 nonsense mutation 52 HNPCC 52 blastomeres 52 lobular carcinoma 52 sCJD 52 developmental abnormalities 52 postpartum hemorrhage 52 microdeletion 52 Fragile X Syndrome 52 Anencephaly 52 Li Fraumeni syndrome 52 de novo mutations 52 nuchal translucency 52 genetic disorder 52 MSH2 52 CIN2 + 52 oligohydramnios 52 BRCA1 mutation carriers 52 omphalocele 52 chromosomally abnormal 52 polycystic ovary syndrome 52 fetal anomalies 52 nodal metastases 52 brain malformation 52 subclinical hyperthyroidism 52 congenital defects 52 grade cervical intraepithelial 52 congenital cytomegalovirus 52 coarctation 52 hamartoma 52 fetal abnormality 52 de ath 52 retinopathy 52 situs inversus 52 neoplasm 52 homozygous 52 autism spectrum disorder 52 neurofibromatosis type 52 germline mutations 51 febrile seizure 51 varicoceles 51 heterozygotes 51 ARVD 51 PCa 51 hepatectomy 51 Kabuki syndrome 51 mutated gene 51 umbilical artery 51 Tetralogy 51 spastic diplegia 51 Brugada syndrome 51 extracolonic findings 51 adenocarcinomas 51 chromosomal alterations 51 endometrial carcinoma 51 IKZF1 51 hypoplastic 51 genetic defect 51 congenital adrenal hyperplasia 51 MECP2 gene 51 IGF2 51 ELBW infants 51 C#Y 51 Hypoplastic Left Heart 51 mitochondrial dysfunction 51 Moyamoya disease 51 RSV infections 51 Meckel Gruber 51 chorioamnionitis 51 carcinoid tumor 51 AAT deficiency 51 neonate 51 chromosomal aberrations 51 conceptus 51 autistic traits 51 normal karyotype 51 phthalate syndrome 51 atrial septal defect 51 Brugada Syndrome 51 lymph node metastases 51 precocious puberty 51 Holoprosencephaly 51 diagnosis PGD 51 colorectal cancer CRC 51 epithelial ovarian cancer 51 tumor recurrence 51 chromosome deletion 51 causative gene 51 breast carcinoma 51 defective gene 51 hyperplasia 51 CNVs 51 dysgenesis 51 oral clefts 51 neoplasias 51 lymphangioleiomyomatosis LAM 51 FXTAS 51 cervical dilation 51 osteopetrosis 51 Pre eclampsia 51 preterm infants 51 HMGA2 51 NNRTI resistance 51 gene mutation 51 proband 51 BRCA mutation carriers 51 triplet pregnancies 51 sickle cell disease 51 embryo biopsy 51 echogenic bowel 51 herpesviruses 51 gene mutations 51 MLL2 51 C#BL/#J 51 medulloblastoma tumors 51 Noonan Syndrome 51 radical nephrectomy 51 NAFLD 51 apolipoprotein E gene 51 neonatal respiratory distress 51 uterine rupture 51 enterocolitis 50 Rh positive 50 chromosome 50 #q#.# deletion syndrome 50 histologic 50 Severe Combined Immunodeficiency 50 growth restriction IUGR 50 maternal serum 50 ischemic lesions 50 endostatin 50 Cushing syndrome 50 recessive inheritance 50 microdeletions 50 fallot 50 autistic regression 50 testis 50 PPCM 50 V Leiden 50 gene variants 50 imprinted genes 50 LRAT 50 infarcts 50 Preeclampsia 50 pyelonephritis 50 gestational age 50 extreme prematurity 50 seropositivity 50 #p#.# [001] 50 POAG 50 neuroblastoma 50 LVNC 50 placenta praevia 50 TMPRSS2 ERG fusion 50 Intussusception 50 recurrent VTE 50 APOL1 50 Polycystic ovary syndrome 50 bladder exstrophy 50 gestational 50 BRCA2 50 corpus luteum 50 cervical carcinoma 50 congenital cataract 50 #q# [001] 50 D dimer 50 karyotyping 50 neurodevelopmental disorder 50 neonatal morbidity 50 Thrombocytopenia 50 DiGeorge syndrome rare 50 codons 50 metabolic disorder 50 mammary tumors 50 dyskeratosis congenita 50 CC genotype 50 sonographic diagnosis 50 familial aggregation 50 congenital CMV infection 50 idiopathic 50 sonographic examination 50 monoclonal gammopathy 50 primary ciliary dyskinesia 50 MYCN amplification 50 Congenital Adrenal Hyperplasia 50 hypospadias 50 biliopancreatic diversion 50 hyperemesis 50 undiagnosed celiac disease 50 neuroblastomas 50 monozygotic twin 50 intrapartum 50 hypopituitarism 50 #q deletion 50 hematuria 50 microvascular disease 50 BRCA2 mutations 50 G6PD 50 neoplasms 50 confidence interval #.#-#.# 50 contrast induced nephropathy 50 lobular breast cancer 50 claudin 50 Krabbe disease 50 fetal echocardiogram 50 #q# deletion 50 macrosomia 50 immunodeficiency 50 KCNE2 50 malignant transformation 50 HER2 gene 50 CFTR gene 50 % CI #.#-#.# [007] 50 somatic mutations 50 brachial plexus palsy 50 adrenalectomy 50 supratentorial 50 preterm babies 50 spinocerebellar ataxia 50 medulloblastomas 50 malperfusion 50 infantile hemangiomas 50 familial hypercholesterolemia 50 mitochondrial disease 50 perinatal asphyxia 50 Rh factor 50 rs# [002] 50 graft dysfunction 50 genetic variant 50 TACI mutations 50 intraoperative complications 50 Chiari malformation 50 axillary lymph nodes 50 recessive genes 50 preterm 50 Alagille syndrome 50 genetic mutation 50 ectodermal dysplasia 50 Cockayne syndrome 50 GH deficiency 50 biochemical recurrence 50 T1DM 50 hyperoxia 50 recurrent miscarriages 50 pericardial effusion 50 prognostic factor 50 atrioventricular septal defect 50 agenesis 50 CNTNAP2 49 BRCA1 gene 49 peripartum cardiomyopathy 49 epididymitis 49 IPAH 49 pneumococci 49 PPHN 49 APOE e4 49 mutations 49 obstetrical complications 49 genetic defects 49 contralateral breast cancer 49 exotropia 49 somatic mutation 49 congenital CMV 49 FDG uptake 49 cerebral infarction 49 coronary artery stenosis 49 antral follicles 49 Crouzon Syndrome 49 systemic amyloidosis 49 anovulatory 49 MLH1 49 unexplained infertility 49 ovarian hyperstimulation 49 hereditary breast cancer 49 periventricular 49 onset diabetes mellitus 49 familial AF 49 skeletal dysplasia 49 prenatal ultrasound 49 neurodevelopmental 49 ultrasonographic 49 sonographically 49 atrial septal defects 49 premature ovarian 49 thyroid hormone levels 49 MTHFR 49 nonischemic 49 recurrent wheezing 49 follicle stimulating hormone 49 brain lesions 49 #q#.# [002] 49 cardioembolic stroke 49 GSTP1 49 placental insufficiency 49 Retinoblastoma 49 endometrial hyperplasia 49 atherosclerotic lesion 49 chorionic villi 49 Klinefelter Syndrome 49 salpingo oophorectomy 49 phenotype 49 familial adenomatous polyposis FAP 49 X chromosome 49 cytologic 49 medium chain acyl 49 ectopic pregnancy 49 Doppler sonography 49 benign lesions 49 Medulloblastoma 49 Krabbe Disease 49 VCFS 49 locoregional recurrence 49 nonsense mutations 49 neurodevelopmental disability 49 maternally inherited 49 hypoperfusion 49 UGT#A# * 49 trimester fetuses 49 PGD PGS 49 precursor lesions 49 JAK mutations 49 invasive carcinoma 49 CMV disease 49 dysplastic 49 malignant nodules 49 invasive meningococcal disease 49 CDH1 49 ovarian carcinoma 49 renal cell carcinomas 49 Gestational diabetes 49 neurological sequelae 49 HGPIN 49 spontaneous preterm delivery 49 MetS 49 bicuspid valve 49 JMML 49 thyroid nodules 49 mammographic density 49 autosomal recessive genetic 49 osteochondromas 49 euthyroid 49 serum IGF 49 microcephaly 49 familial adenomatous polyposis 49 SIDS infants 49 premutation 49 hyperemesis gravidarum 49 chromosome #q#.# [001] 49 μg dL 49 birth defect 49 RSV bronchiolitis 49 cardiac dysfunction 49 parasitaemia 49 placenta previa 49 histopathologic examination 49 beta globin gene 49 asplenia 49 PALB2 49 perioperative complications 49 renovascular hypertension 49 Wolf Hirschhorn 49 septo optic dysplasia 49 Legg Calvé Perthes disease 49 onset sepsis 49 leptin receptor 49 vesicoureteral reflux 49 atopy 49 noncardiac 49 CHD7 49 chromosomal imbalance 49 autoantibodies 49 adenomas 49 gestational diabetes mellitus 49 APOE gene 49 spontaneous remission 49 ovulations 49 HELLP syndrome 49 pathogenic mutations 49 SHANK3 49 fibrous dysplasia 49 esophageal atresia 49 histiocytosis 49 distant metastases 49 invasive cervical cancer 49 ovarian hyperstimulation syndrome OHSS 49 hypogonadotropic hypogonadism 49 TCF#L# gene 49 transcranial Doppler 49 neonatal encephalopathy 49 X inactivation 49 neuropsychiatric disorder 49 nucleotide substitutions 49 Recurrences 49 Fanconi Anemia 49 mitochondrial diseases 49 thymectomy 49 epithelial tumors 49 bilirubin levels 49 neurodegenerative disorder 49 BRCA2 mutation 49 neurologic complications 49 malignant fibrous histiocytoma 49 uterine tumors 49 chromosomal deletions 49 pathologic 49 dilated cardiomyopathy 49 renal scarring 49 Gestational 49 chromosomal rearrangements 49 retinal dysfunction 49 Low birthweight 49 chronic granulomatous disease 49 MALT lymphoma 49 genes BRCA1 49 FASPS 49 YKL 49 hemangioma 48 myeloproliferative neoplasms 48 gastric carcinoma 48 endometrial 48 Leber Congenital Amaurosis LCA 48 preeclamptic women 48 advanced adenomas 48 PTPN# 48 multivariable analysis 48 frameshift mutation 48 idiopathic scoliosis 48 myelination 48 prenatally 48 neuroblastoma tumors 48 PSADT 48 % CI #.#-#.# [004] 48 Down syndrome chromosomal disorder 48 patent ductus arteriosus 48 anomalous pulmonary venous 48 tumoral 48 ovarian dysfunction 48 vasa previa 48 Osteosarcoma 48 neurodevelopmental disorders 48 endometritis 48 biventricular repair 48 multivariate Cox 48 BRCA mutation 48 histologically 48 MYH9 gene 48 Myocardial infarction 48 noncarriers 48 congenital abnormality 48 Arnold Chiari Malformation 48 heritable 48 preimplantation genetic diagnosis 48 singleton babies 48 cri du chat 48 astrocytomas 48 antenatal depression 48 embryo 48 glucose tolerance test 48 K#N 48 ovarian hyperstimulation syndrome 48 placenta accreta 48 tuberous sclerosis complex 48 G6PD deficiency 48 ovulatory cycles 48 Hutchinson Gilford progeria 48 perinatal mortality 48 bronchiolitis 48 respiratory distress syndrome 48 cerebellar hypoplasia 48 chromosomal mutations 48 Stillbirth 48 Newborn screening 48 VLBW infants 48 SLNB 48 ELBW 48 HFE gene 48 % CI #.#-#.# [003] 48 intracytoplasmic sperm injection 48 intracytoplasmic 48 #.#ng/ml 48 definite stent thrombosis 48 hypoxemia 48 cystic fibrosis muscular dystrophy 48 recessive gene 48 allelic variants 48 IL#B 48 oophorectomy 48 intrauterine 48 SUVmax 48 Aneuploidy 48 bladder tumors 48 ovulation induction 48 EGFR gene 48 mutated BRCA1 48 quadruplet births 48 endocrine disorder 48 histopathologic 48 mesotheliomas 48 polycystic kidneys 48 Prox1 48 BRCA2 carriers 48 Chromosome 48 sarcomatoid 48 testicular tumors 48 spontaneously aborted 48 recessive genetic disorders 48 fraternal triplets 48 ductal 48 fetal echocardiography 48 node metastases 48 dominantly inherited 48 ovarian malignancy 48 5q 48 Sonographic 48 transvaginal sonography 48 intrauterine pregnancy 48 Leber congenital amaurosis LCA 48 paraganglioma 48 prematurity ROP 48 RSV infection 48 mucinous 48 neonates 48 autosomal recessive disease 48 cystic lesions 48 phenylketonuria 48 homozygous familial hypercholesterolemia 48 hydroxyvitamin D 48 chlamydial infection 48 APOE 48 toxemia 48 #p#.# [002] 48 diabetes mellitus T2DM 48 birthweight 48 bicuspid aortic valve 48 pneumonectomy 48 polyposis 48 retinoblastoma 48 5 methylcytosine 48 AAT Deficiency 48 hemorrhagic complications 48 embryo implantation 48 pulmonary stenosis 48 HGPS 48 spinal muscle atrophy 48 BRCA2 gene 48 amnion 48 Dysplasia 48 allele 48 Uterine fibroids 48 long QT syndrome 48 confidence interval CI 48 autosomal recessive disorder 48 airway hyperresponsiveness 48 deleterious mutation 48 CGG repeats 48 probands 48 PDGFRA 48 prion disease 48 gene expression patterns 48 necrotising enterocolitis 48 ichthyosis 48 haplotype 48 factor PlGF 48 transabdominal 48 Rb gene 48 BRCA1 mutation 48 von Willebrand disease 48 noninvasive prenatal 48 hydrocephaly 48 hereditary nonpolyposis colorectal cancer 48 gestational hypertension 48 polycystic disease 48 microchimerism 48 #p# [001] 48 Metastases 48 breast cancers 48 craniopagus parasiticus 48 VLBW 48 lobular cancer 48 obstructive coronary artery 48 nonhereditary 48 Spinal muscular atrophy 48 cerebral vasospasm 48 endometrioid 48 Leber congenital amaurosis 48 #q# deletion syndrome 48 benign polyps 48 colorectal neoplasms 48 benign growths 48 fraternal twin pairs 48 pneumococcal infection 48 cryptogenic stroke 48 eosinophilic 48 postoperative pulmonary 48 radioiodine therapy 48 tyrosine phosphorylation 48 invasive breast cancer 48 ependymomas 48 parathyroid 48 5q deletion 48 preoperative PSA 48 CagA 48 Twin Transfusion Syndrome 48 TT genotype 48 neural tube birth defects 48 haplotypes 48 cTnT 48 preeclamptic 48 assisted reproduction 47 tuberculous 47 adrenal insufficiency 47 ductal breast cancer 47 proximal colon 47 Sandhoff disease 47 methylation 47 achromatopsia 47 newborn infants 47 cytogenetic abnormalities 47 pleural mesothelioma 47 stillbirth 47 subclinical atherosclerosis 47 egg follicles 47 neuroblastoma tumor 47 smoldering myeloma 47 sensorineural hearing loss 47 intrauterine infection 47 venous thrombosis 47 PDD NOS 47 mRNA expression 47 WAGR syndrome 47 primary pulmonary hypertension 47 cardiomegaly 47 nmol L 47 SMN1 47 intestinal biopsy 47 operable breast cancer 47 basal cell carcinomas 47 lacunar 47 tuberous sclerosis 47 BCL#A 47 Neurofibromatosis type 47 abnormality 47 Adenomas 47 carotid stenosis 47 osteogenesis imperfecta 47 gestational sac 47 elevated CRP 47 T2DM 47 ruptured aneurysms 47 Aortic stenosis 47 catheter angiography 47 diabetes mellitus DM 47 rs# [004] 47 euthymic patients 47 colorectal carcinoma 47 amnio 47 aneuploid cells 47 Lafora disease 47 adrenal function 47 nuchal fold 47 dimensional sonography 47 Apgar scores 47 fibroma 47 nulliparous 47 biopsied embryos 47 intracytoplasmic sperm injection ICSI 47 plain radiographs 47 Eclampsia 47 eclampsia 47 mammary cells 47 breastfed exclusively 47 malignancy 47 normal birthweight 47 cystic hygroma 47 Clusterin 47 elevated triglyceride levels 47 precancerous cervical 47 hyperparathyroidism 47 pregnancies 47 spontaneous vaginal 47 esophageal carcinoma 47 pituitary adenomas 47 unexplained mental retardation 47 FGFR2 47 allelic 47 radiographic findings 47 juvenile myelomonocytic leukemia 47 Fragile X gene 47 cardiac tamponade 47 esotropia 47 osteochondroma 47 Sanfilippo Syndrome 47 NOTCH1 47 tricuspid valve 47 BRCA carriers 47 susceptibility gene 47 gonadotropins 47 choroidal neovascularization CNV 47 Premature infants 47 retinal degeneration 47 necrotizing enterocolitis NEC 47 neurodevelopmental outcomes 47 dysmorphic features 47 neonatal sepsis 47 Heavy menstrual bleeding 47 Polycystic ovarian syndrome 47 breast cancer genes BRCA1 47 BRCA genes 47 metastases 47 pheochromocytoma 47 homozygote 47 SRBD 47 cause cardiac channelopathies 47 xeroderma pigmentosum 47 hypoxic ischemic encephalopathy 47 ductal cancer 47 mitochondrial mutations 47 colorectal neoplasia 47 BLLs 47 breech babies 47 IDDM 47 Loeys Dietz syndrome 47 colorectal polyps 47 CHEK2 47 nonmelanoma skin cancers 47 TEL AML1 47 pre cancerous lesion 47 thalassemia trait 47 cardiac hypertrophy 47 renal agenesis 47 pheochromocytomas 47 FSGS 47 Prematurity 47 germline cells 47 G#S mutation 47 albuminuria 47 aplasia 47 Inhibin B 47 STAT4 47 chlamydial 47 single nucleotide polymorphism 47 hTERT 47 thyroid dysfunction 47 rare congenital defect 47 p# mutation 47 born prematurely 47 nonmelanoma skin cancer 47 severe congenital neutropenia 47 liver metastasis 47 MC1R 47 neural tube defects NTDs 47 HRCT 47 transgene expression 47 congenital cardiac 47 primitive neuroectodermal tumors 47 enterovirus infection 47 overt hypothyroidism 47 Nonsense mutations 47 chromosomally normal 47 neural tube 47 asymptomatic 47 mitral regurgitation 47 Haptoglobin 47 MMP# 47 lung lesions 47 pCR 47 bowel cancers 47 LTBI 47 proto oncogene 47 post natally 47 vasogenic edema 47 spontaneous mutations 47 VNTR 47 troponin T 47 low birthweight infants 47 immunodeficiencies 47 peripartum 47 pseudotumor cerebri

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