chromosome abnormalities

Related by string. * Chromosome . Chromosomes . chromosomes : Y chromosome . chromosome #q# [001] . chromosome #q# [002] . inactive X chromosome . aY chromosome . chromosome aberrations / Abnormalities : additional cytogenetic abnormalities . fetal abnormalities . rhythm abnormalities . physiological abnormalities . chromosomal abnormalities . congenital abnormalities * *

Related by context. All words. (Click for frequent words.) 72 chromosomal abnormalities 69 aneuploidies 68 genetic abnormalities 67 aneuploidy 65 somatic mutations 65 congenital anomalies 65 holoprosencephaly 64 chromosomal anomaly 64 chromosomal aberrations 64 recurrent miscarriages 64 de novo mutations 64 chromosomal disorders 64 chromosomal anomalies 63 mosaicism 63 developmental abnormalities 63 inherited mutations 63 chromosome abnormality 63 fetal chromosomal 62 abnormalities 62 microdeletion 62 IgA deficiency 61 HbF 61 sCJD 61 neural tube defect 61 mtDNA mutations 61 chromosome rearrangements 61 chromosomal rearrangement 61 methylation markers 61 transfusion syndrome 60 preterm deliveries 60 genomic deletions 60 fetal aneuploidy 60 microdeletions 60 MCAD deficiency 59 CHD7 59 spontaneous mutations 59 aneuploidy screening 59 congenital abnormalities 59 normal karyotype 59 genomic rearrangements 59 fetal chromosomal abnormalities 59 sporadic ALS 59 genetic defects 59 mitochondrial dysfunction 59 congenital malformations 59 polycystic ovary syndrome PCOS 59 causative gene 59 genetic abnormality 59 #q# deletion 59 neurological abnormalities 59 epigenetic changes 59 dizygotic twins 59 SHANK3 58 APOE e4 58 abnormal chromosomes 58 familial ALS 58 G#S mutation 58 Beckwith Wiedemann syndrome 58 pathogenic mutations 58 mutations 58 Rh incompatibility 58 #q#.# [001] 58 blastomeres 58 NR#A# gene 58 splice junctions 58 hamartomas 58 thrombophilia 58 embryo biopsy 58 chromosomal defect 58 LRRK2 gene 58 pre eclamptic 58 fetal malformations 58 MSH2 58 trisomy 58 chorionic villi 58 FGFR2 gene 58 chromosomally abnormal 58 diagnostic biomarker 58 chromosomal defects 58 genetic defect 58 missense mutations 57 aneuploid 57 Cytogenetic 57 ependymoma 57 unexplained infertility 57 prenatally diagnosed 57 DNA methylation patterns 57 Folic acid deficiency 57 ependymomas 57 germline mutations 57 INF2 57 breast cancer genes BRCA1 57 JAK mutations 57 genetic syndromes 57 somatic mutation 57 fetal abnormalities 57 MeCP2 gene 57 Chromosomal abnormalities 57 chromosomal instability 57 KRAS oncogene 57 lung lesions 57 mitochondrial DNA mtDNA 57 promoter hypermethylation 57 recurrent miscarriage 57 filaggrin 57 neurodevelopmental disorder 57 epigenetic alterations 57 hyperinsulinism 57 IUGR 57 postnatally 57 PGD PGS 57 FMR1 gene 57 ALK mutations 57 BRCA1 mutations 57 chromosomal alterations 57 chromosomal disorder 57 chromosome #q#.# [001] 57 MCADD 57 achromatopsia 57 chromosomal deletions 57 chromosomal abnormality 57 GBA mutations 56 mammographically 56 MLH1 56 LQTS 56 monogenic 56 maternally inherited 56 spontaneous mutation 56 CNVs 56 mitochondrial disorders 56 diagnosed prenatally 56 hydrops 56 phthalate syndrome 56 Klinefelter syndrome 56 familial clustering 56 PALB2 56 neuroblastomas 56 FMR1 56 karyotype 56 gene mutations 56 #q#.# [002] 56 SMN protein 56 clefting 56 chromosomal rearrangements 56 MECP2 gene 56 BRCA1 BRCA2 56 chromosomal mutations 56 brain lesions 56 chromosomal imbalance 56 Rh factor 56 karyotypes 56 #q#.# deletion syndrome 56 M. genitalium 56 Brugada syndrome 56 medulloblastomas 56 epigenetic modification 56 Velculescu 56 herpesviruses 56 LRRK2 mutations 56 CMV infection 56 BRIP1 56 autosomal dominant inheritance 56 CHDs 56 WDR# 56 TCF#L# gene 56 intrauterine infection 56 MYCN amplification 56 gestational diabetes mellitus 56 heterotaxy 56 BRCA2 gene 56 genetic rearrangements 56 causative mutation 56 K ras mutations 56 ovarian hyperstimulation 56 galactosemia 56 IVF ICSI 56 colorectal neoplasia 56 chromosome translocations 56 BRCA1 gene 56 de ath 56 mitochondrial diseases 56 NF1 56 methylation patterns 56 exome sequencing 55 mutant genes 55 neurodevelopmental disorders 55 3'UTR 55 Meckel Gruber 55 BARD1 55 malformations 55 nonhereditary 55 Preimplantation genetic diagnosis 55 congenital disorders 55 precursor lesions 55 epigenetic markers 55 hereditary breast cancer 55 BRCA2 gene mutation 55 leptin deficiency 55 dyskeratosis congenita 55 MeCP2 protein 55 p# mutations 55 polydactylism 55 anovulation 55 renal cell carcinomas 55 FGFR2 55 mitochondrial defects 55 non coding RNA 55 metabolic abnormalities 55 array CGH 55 gene mutation 55 MLL2 55 PTPN# 55 Pten 55 biochemical abnormalities 55 endometrial cancers 55 chlamydial infection 55 microRNA expression 55 VHL gene 55 intracytoplasmic sperm injection 55 congenital toxoplasmosis 55 chorioamnionitis 55 Apert syndrome 55 atypical hyperplasia 55 imprinted genes 55 Fanconi anemia 55 BRCA gene mutation 55 shortened telomeres 55 prion infection 55 metabolomic profiles 55 causative genes 55 enterovirus infection 55 motor neuron degeneration 55 IKZF1 55 causal variants 55 congenital adrenal hyperplasia CAH 55 mutant allele 55 micro RNAs 55 molecular abnormalities 55 endostatin 55 biopsied embryos 55 genetic mutations 55 nonsense mutations 55 neuro developmental disorders 55 PTEN gene 55 teratoma 55 KRAS mutations 55 hypermethylated 55 Fragile X gene 55 karyotyping 55 hamartoma 55 monozygotic twins 55 autistic traits 55 #p#.# [002] 55 mitochondrial mutations 55 abnormal prions 55 malignant polyps 55 CDH1 55 Clusterin 55 gene rearrangements 55 chromosome aberrations 55 pilocytic astrocytomas 55 connexin 55 polycystic ovaries 55 CIN2 + 55 HNPCC 54 sonographic diagnosis 54 mutation 54 precancerous tumors 54 gastric carcinoma 54 HGPS 54 LIS1 54 penetrance 54 methylated DNA 54 uniparental 54 protein encoded 54 PTEN mutations 54 congenital CMV 54 neurosensory 54 placental malaria 54 pancreatic endocrine 54 adnexal mass 54 Cowden syndrome 54 #p# [001] 54 DNA methylation 54 breast carcinomas 54 sequence homology 54 epithelial tissues 54 genital tract infections 54 NGAL 54 mutant alleles 54 familial pancreatic cancer 54 myopathies 54 histocompatibility 54 orofacial clefts 54 autism susceptibility genes 54 CNTNAP2 54 causative mutations 54 prenatal diagnosis 54 Male infertility 54 HMGA2 54 persistent pulmonary hypertension 54 microRNA molecules 54 Li Fraumeni syndrome 54 genetic variants associated 54 reproductive endocrine 54 lissencephaly 54 #p#.# [001] 54 chromosome deletion 54 Six3 54 G6PD deficiency 54 BRCA carriers 54 genetic alterations 54 vitro maturation 54 genomewide 54 Angelman syndrome 54 SOD1 gene 54 genetic variant 54 genomic variants 54 phthalate exposure 54 beta thalassemia 54 mRNA transcripts 54 APOL1 54 microsatellite instability 54 bronchopulmonary dysplasia 54 renal scarring 54 molar pregnancy 54 progranulin gene 54 cybrid 54 neurodevelopmental 54 mutated K ras 54 abnormal methylation 54 thyroid hormone levels 54 SMN2 54 gene variants 54 phylogenetic analyzes 54 nucleotide substitutions 54 impair fertility 54 immunodeficiencies 54 genomic alterations 54 ovulatory cycles 54 mammary cells 54 chromosomal 54 mutated BRCA1 54 genetic imprinting 54 GFP gene 54 SORL1 54 cytogenic 54 Joubert syndromes 54 gene amplification 54 spontaneous miscarriages 54 autosomal 54 BRCA2 carriers 54 neurologic complications 54 Ebstein anomaly 54 beta1 integrin 54 varicoceles 54 epigenetic silencing 54 placenta praevia 54 egg follicles 54 alpha synuclein gene 54 TGFBR1 * 6A 54 IDH1 mutation 54 mesotheliomas 54 #q# [001] 54 amyloid deposition 54 facial clefts 54 heterozygotes 54 shorter telomeres 54 inhibin B 54 Epstein Barr virus EBV 54 EBV infection 54 X chromosome inactivation 54 advanced neoplasia 54 aneuploid cells 54 reproductive abnormalities 54 chromosomal translocations 54 neuroblastoma tumors 54 thyroid carcinoma 54 ovarian hormones 54 polycystic ovary syndrome 54 cytogenetic 54 polyploidy 54 KCNH2 54 IDH mutations 54 behavioral disinhibition 54 thyroid nodules 54 virulence genes 54 Genetic mutations 54 Leydig cell 54 CHEK2 54 mammary cancers 54 dysmorphic features 54 medium chain acyl 53 thiopurine 53 familial aggregation 53 PARP inhibition 53 ultra rapid metabolizer 53 Genetic variants 53 PDGFRA 53 ERK2 53 PIK3CA 53 Alu elements 53 NPHP 53 Rb gene 53 BRCA2 mutations 53 phthalate metabolites 53 mice lacking 53 mammary tumors 53 testicular tumors 53 B7 H3 53 IVF pregnancies 53 EoE 53 SLITRK1 53 gene expression patterns 53 myelomeningocele 53 born preterm 53 endocrine abnormalities 53 ectopic pregnancies 53 granule cells 53 ovarian function 53 HLA typing 53 spontaneously aborted 53 progranulin 53 GPC5 53 APOE ε4 53 ZNF# 53 ductal breast cancer 53 ambiguous genitalia 53 dysbindin gene 53 SCN5A 53 triplet pregnancies 53 ADPKD 53 Sjögren syndrome 53 advanced adenoma 53 aplasia 53 congenital deafness 53 Reefhuis 53 GISTs 53 genetic polymorphisms 53 MYH9 gene 53 gene expression microarray 53 ASDs 53 alpha thalassemia 53 CFTR gene 53 basal cell nevus syndrome 53 genotoxic stress 53 malignant lesions 53 TP# mutation 53 RT PCR assay 53 varicella infection 53 choriocarcinoma 53 microchimerism 53 anovulatory infertility 53 ovarian malignancy 53 Kufs disease 53 leiomyoma 53 JMML 53 genetic mutation 53 embryonal 53 APOE gene 53 prion infections 53 lobular cancer 53 gene BRCA2 53 genes BRCA1 53 ORMDL3 53 mutated gene 53 leiomyomas 53 Jhdm2a 53 maternally transmitted 53 LRP5 53 HLA genes 53 onset sepsis 53 aCGH 53 ovarian tumors 53 polyhydramnios 53 Leydig cells 53 ipRGCs 53 prenatal ultrasound 53 Genetic predisposition 53 cytogenetic abnormalities 53 TMEM#B 53 MAPCs 53 differential gene expression 53 TOP2A 53 antiphospholipid antibodies 53 lobular breast cancer 53 Kabuki syndrome 53 miRNA genes 53 RSV bronchiolitis 53 MC4R gene 53 neuroligins 53 Hashimoto thyroiditis 53 monozygotic 53 apoE 53 TYMS 53 VNTR 53 CNTNAP2 gene 53 heterozygous 53 cytologic 53 KRAS BRAF 53 autosomal recessive 53 gene MECP2 53 premature menopause 53 ectopic 53 Down syndrome spina bifida 53 allelic variants 53 anencephaly 53 matriptase 53 5q 53 HHV 6 53 extracolonic findings 53 TP# gene 53 Ets2 53 adrenal tumors 53 preimplantation genetic diagnosis 53 congenital hypothyroidism 53 maternal serum 53 colonic polyps 53 cardiac troponin 53 neurofibromas 53 defective gene 53 LPA receptors 53 childhood leukemias 53 bowel cancers 53 abnormal proteins 53 thyroglobulin 53 primordial germ cells 53 haematopoietic 53 mutated genes 53 L. pneumophila 53 neoplasm 53 behavioral abnormalities 53 hemolytic disease 53 male infertility 53 genes predisposing 53 tumor suppressor protein 53 Hurthle cell 53 VCFS 53 Cockayne syndrome 53 genomic loci 53 cytomegalovirus infection 53 ALK gene 53 telomere lengths 53 CISH 52 nucleotide variations 52 FXTAS 52 exomes 52 urine cytology 52 Peutz Jeghers syndrome 52 DNA rearrangements 52 osteosarcomas 52 adenomatous polyps 52 precancerous cervical 52 sarcosine 52 affective psychoses 52 predisposing factor 52 hypopituitarism 52 thyroid abnormalities 52 testicular biopsy 52 NF2 52 pulmonary hypoplasia 52 immunohistochemical 52 MC1R 52 genital abnormalities 52 ApoE4 gene 52 primary ovarian insufficiency 52 thyrotropin levels 52 TMPRSS2 ERG 52 trophoblast 52 monozygotic twin 52 dominantly inherited 52 noncoding RNAs 52 oocytes eggs 52 narcolepsy cataplexy 52 microRNAs miRNAs 52 undiagnosed celiac disease 52 splice variants 52 ovarian dysfunction 52 postoperative complication 52 Irva Hertz Picciotto 52 Hurler syndrome 52 N. gonorrhoeae 52 adenoma 52 methylation 52 unexplained mental retardation 52 homozygosity 52 Li Fraumeni 52 Hakonarson 52 OGG1 52 pituitary hormone 52 poorer prognosis 52 KCNE2 52 overdiagnosis 52 GATA4 52 phenotypic expression 52 intraventricular hemorrhage 52 cystic fibrosis muscular dystrophy 52 fertilized egg splits 52 fronto temporal dementia 52 indel 52 azoospermia 52 Joubert syndrome 52 cholestasis 52 trophoblast cells 52 phenotypic variation 52 BCL#A 52 colorectal cancer CRC 52 activating mutations 52 ERBB2 52 5q deletion 52 neurodevelopmental outcomes 52 fetal echocardiography 52 mtDNA 52 nulliparous 52 MTHFR 52 PON1 52 neonatal morbidity 52 chimerism 52 genomewide association studies 52 telomere DNA 52 BRAF gene 52 neonatal encephalopathy 52 Prox1 52 hypogonadotropic hypogonadism 52 diagnosis PGD 52 p# activation 52 gene deletions 52 paralogs 52 auditory neuropathy 52 genetic heterogeneity 52 FMRP protein 52 abnormal Pap smear 52 ovulated 52 situ hybridization 52 neuropsychological impairments 52 HLA DRB1 52 fibroma 52 chromosomally normal 52 macaque genome 52 NNRTI resistance 52 UGT#A# * 52 Chromosomal 52 TMPRSS2 ERG fusion 52 SHANK3 gene 52 HPRT gene 52 axillary dissection 52 myotonic dystrophy 52 body louse genome 52 Retinopathy 52 pathologic examination 52 Meckel Gruber syndrome 52 acute lymphoid leukemia 52 micrometastasis 52 curable cancers 52 Beta thalassemia 52 paraneoplastic 52 asymptomatic carriers 52 glutamic acid decarboxylase 52 pre cancerous lesions 52 Dravet syndrome 52 Amniocentesis 52 mammary gland tumors 52 RhD negative 52 previously uncharacterized 52 RNA ribonucleic acid 52 mitochondrial proteins 52 CIN3 52 T1DM 52 ataxias 52 N myc 52 morphological abnormalities 52 mammographic density 52 genomic instability 52 genetic disorders 52 polycystic kidneys 52 thyroid cancers 52 microcephalin 52 fibroids endometriosis 52 XMRV virus 52 proto oncogene 52 subfertility 52 genomic rearrangement 52 leukaemias 52 Trisomy 52 highly heritable 52 misregulation 52 genomic imprinting 52 genetic loci 52 inactivating mutations 52 bladder tumors 52 SMN1 52 mammalian embryos 52 neuro developmental 52 medulloblastoma tumors 52 von Hippel Lindau 52 DiGeorge syndrome 52 immunoreactivity 52 BRCA mutation carriers 52 autosomal dominant 52 craniofacial anomalies 52 NFKBIA 52 podocytes 52 vesicoureteral reflux VUR 52 congenital adrenal hyperplasia 52 miRNAs 52 MLL gene 52 genetic alteration 52 preeclamptic women 52 histopathologic 52 neurological complications 52 micro RNA 52 hyperplastic 52 perinatal outcomes 52 leukoencephalopathy 52 pituitary tumors 52 troponin T 52 Dr. Loeken 52 susceptibility gene 52 Karayiorgou 52 tau mutation 52 advanced adenomas 52 NAFLD 52 CagA 52 autosomal dominant disorder 52 perinatal asphyxia 52 Noonan Syndrome 52 VUR 52 prostate carcinogenesis 52 Circulating tumor cells 52 thoracic aortic disease 52 epigenetic mechanisms 52 HER2 gene 52 susceptibility genes 52 autistic regression 52 promoter methylation 52 bacteraemia 52 perilipin 52 heterozygosity 52 situs inversus 52 multiple gestations 52 deafness neurological 51 proband 51 recessive genes 51 genetic locus 51 inherited predisposition 51 subtyped 51 nodal metastases 51 colocalization 51 indels 51 lung adenocarcinoma 51 severe congenital neutropenia 51 Cyclin D1 51 IGF2 51 gene expression profiles 51 folate metabolism 51 gene APOE4 51 neurodevelopmental impairment 51 incidentalomas 51 amniotic cells 51 single nucleotide polymorphism 51 pancreatic tissue 51 Wwox 51 Pre implantation genetic 51 deCODE BreastCancer TM 51 CDKN2A 51 HER2 amplification 51 Spinal muscular atrophy 51 primary cilia 51 C. pneumoniae 51 antenatal depression 51 skeletal malformations 51 p# mutation 51 neoplasms 51 hypoplasia 51 androgen receptor gene 51 chlamydial infections 51 etiologic 51 utero exposure 51 transgene expression 51 microarray experiments 51 embryonic tissues 51 endometrioid 51 inactive X chromosome 51 pathologic diagnosis 51 RKIP 51 fetal anomalies 51 SLC#A# [002] 51 MYH9 51 mutant huntingtin protein 51 intracytoplasmic 51 APOE4 51 familial adenomatous polyposis 51 meningiomas 51 BRAC2 51 chimeric mice 51 peripartum cardiomyopathy 51 serologic 51 carcinoid tumor 51 chromosome #q# [002] 51 hereditary deafness 51 miRNA expression 51 NSCLC tumors 51 UVB induced 51 hyperbilirubinemia 51 SMN2 gene 51 PTEN protein 51 hormonal stimulation 51 genomic profiling 51 singleton pregnancy 51 POAG 51 Fetal heartbeats 51 ductal carcinomas 51 uterine cancers 51 inheritable genetic 51 hypermethylation 51 alleles 51 spontaneous abortions 51 benign growths 51 bowel polyps 51 filaggrin gene 51 recessive inheritance 51 endometrial carcinoma 51 LKB1 51 immunodeficiency 51 TTTS 51 LRAT 51 mitochondrial genomes 51 cranial radiation 51 genetic polymorphism 51 intra uterine 51 neuronal dysfunction 51 MGUS 51 retinal vascular 51 allele frequencies 51 Apobec3 51 Newborn screening 51 molecular biomarkers 51 primary biliary cirrhosis 51 chlamydial 51 PrPSc 51 parthenogenetic 51 prenatally 51 Aneuploidy 51 viral etiology 51 underdiagnosis 51 dystrophin gene 51 hydronephrosis 51 glycosylation 51 da mage 51 singleton pregnancies 51 polymorphic ventricular tachycardia 51 homozygous 51 FGF signaling 51 ABCB1 51 atherosclerotic lesions 51 intraoperative complications 51 intelligence quotient IQ 51 epigenetic regulation 51 DEAR1 51 FOXP3 51 Immunohistochemical analysis 51 Congenital Adrenal Hyperplasia 51 germ cells 51 cloned primate 51 neuropsychiatric diseases 51 hypomethylation 51 thyroid function 51 noncardiac 51 genetic variants 51 Rett syndrome 51 malignant transformation 51 placenta accreta 51 febrile seizures 51 M. pneumoniae 51 metalloprotease 51 varicocele 51 orthologs 51 congenital blindness 51 Hutchinson Gilford progeria 51 non coding RNAs 51 recessive trait 51 structural abnormalities 51 GRP# 51 RUNX3 51 spinocerebellar ataxia 51 Multivariate analysis 51 engineered urethras 51 tumor suppressor gene 51 distant metastasis 51 GIST tumors 51 testicular germ cell 51 postoperative delirium 51 chorionic villus sampling 51 DQB1 * 51 overt hypothyroidism 51 untreated celiac disease 51 prion disease 51 homocystinuria 51 teratogens 51 seropositivity 51 undescended testicles 51 HLA DQ2 51 Fanconi Anemia 51 neuro developmental disorder 51 primary ciliary dyskinesia 51 nephrogenic 51 defects CHDs 51 myeloperoxidase 51 nonmelanoma skin cancers 51 XMRV infection 51 FTLD 51 cranial irradiation 51 Mitochondrial diseases 51 pituitary adenoma 51 transcriptome profiling 51 missense mutation 51 RPE# 51 tumoral 51 ductal adenocarcinoma 51 supratentorial 51 uveal melanoma 51 scintigraphic 51 guinea pigs lubiprostone 51 MAPK pathway 51 deletion 5q 51 lung nodules 51 cerebral angiography 51 Akt1 51 bronchopulmonary dysplasia BPD 51 thyroid dysfunction 51 medulloblastoma 51 bladder cancers 51 BRCA mutations 51 bilirubin levels 51 Folate deficiency 51 chest radiographs 51 Tay Sachs Disease 51 BRCA2 gene mutations 51 abnormal cytology 51 tissue biopsies 51 C1q 51 IPAH 51 recessive mutation 51 leptin receptors 51 Wiskott Aldrich syndrome 51 dysgenesis 51 Levy Lahad 51 urolithiasis 51 preeclamptic 51 gastric carcinomas 51 dose ionizing radiation 51 cancerous polyps 51 stratifying patients 51 vesicoureteral reflux 51 vasa previa 51 generalized vitiligo 51 EGFR gene 51 congenital birth defects 51 breast cancer subtypes 51 ovules 51 rs# [001] 51 NPM1 mutations 51 BRCA2 mutation 51 TRAF1 C5 51 CYP#D# gene 51 hereditary predisposition 51 systemic amyloidosis 51 CYP#B# 51 vascular dysfunction 51 DICER1 51 microscopic hematuria 51 pre malignant lesions 51 herpes infection 51 dedifferentiation 51 abnormal Pap test 51 cyclin E 51 parkin gene 51 histologic 50 enterotypes 50 bicuspid valve 50 embryonic germ 50 untreated hypothyroidism 50 retrovirus XMRV 50 congenital anomaly 50 penile cancers 50 enterocolitis 50 BRCA2 50 microvascular disease 50 neuroinflammation 50 neurocognitive deficits 50 CYP#D# genotype 50 pyloric stenosis 50 Malignant tumors 50 pelvic ultrasound 50 urine dipstick 50 syngeneic 50 benign polyps 50 lymphatic vasculature 50 #.#ng/ml

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