Related by context. All words. (Click for frequent words.) 62 SHANK3 61 autosomal dominant disorder 61 CHD7 60 myopathies 60 COL#A# 60 inherited mutations 60 LRAT 60 pancreatic endocrine 60 Spinal muscular atrophy 59 fibrillin 1 59 CDH1 59 c KIT 59 MECP2 gene 59 dystrophin protein 59 WAGR syndrome 59 progranulin gene 59 ABCB1 59 LKB1 58 IRF6 58 MLH1 58 MEF2A 58 motor neuron degeneration 58 p# mutations 58 Smad3 57 clefting 57 apoE4 57 GATA4 57 Beta thalassemia 57 missense mutation 57 dyskeratosis congenita 57 FUS1 57 JAK2 enzyme 57 MLL2 57 KRAS oncogene 57 #q#.# [002] 57 adipogenic 57 ALK gene 57 epigenetic regulation 57 Clusterin 57 caveolin 57 Prox1 57 DGAT1 57 K ras mutations 56 dysbindin 56 missense mutations 56 nerve degeneration 56 UGT#B# 56 LRP5 56 biochemical abnormalities 56 Pten 56 systemic amyloidosis 56 UGT#A# * 56 abnormal p# 56 neuroD2 56 IgA deficiency 56 filaggrin 56 hypoplasia 56 PTEN gene 56 VHL gene 56 dominantly inherited 56 heterotaxy 56 primary ciliary dyskinesia 56 PTPN# 56 HFE gene 56 SMN2 gene 56 connexin 55 Karayiorgou 55 nonhereditary 55 immunodeficiencies 55 monogenic 55 E#F# 55 desmin 55 PARP inhibition 55 neurological abnormalities 55 SMN protein 55 Neurofibromatosis type 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 VIPR2 55 pituitary adenoma 55 FGFs 55 Heterozygous 55 osteogenesis imperfecta 55 #q# deletion 55 autosomal dominant inheritance 55 SOD1 gene 55 SMN1 55 #q# [001] 55 Hutchinson Gilford progeria 55 LIS1 55 TMPRSS2 ERG fusion 55 thyroid carcinoma 55 cerebri 55 dorsal root ganglia 55 undergo apoptosis 55 cytogenetic abnormalities 54 HLA DR4 immune 54 homeobox 54 functional polymorphism 54 lung fibrosis 54 activating mutations 54 aggrecan 54 pulmonary hypoplasia 54 autosomal recessive disease 54 Vangl2 54 protein encoded 54 KIAA# 54 splice variants 54 DEAR1 54 BRAF gene 54 brain lesions 54 FGFR2 54 HRAS 54 CFTR gene 54 MTHFR 54 embryonal rhabdomyosarcoma 54 neurofibromas 54 microdeletion 54 mutated K ras 54 Brugada Syndrome 54 achromatopsia 54 RPE# 54 TMPRSS2 ERG 54 MSH2 54 chromosomal aberrations 54 replicon 54 CYP#C# [002] 54 de novo mutations 54 dystrophin gene 54 Chronic pancreatitis 54 eotaxin 54 TOP2A gene 54 apolipoprotein E APOE 54 BCR ABL protein 54 CFH gene 53 #p#.# [002] 53 alpha synuclein gene 53 pathogenic mutations 53 chromosome #q#.# [001] 53 FMR1 53 SMN1 gene 53 radiographic findings 53 Eisenmenger syndrome 53 TCF#L# gene 53 NFKBIA 53 NF1 gene 53 familial adenomatous polyposis FAP 53 aneuploidies 53 platelet dysfunction 53 ribosomal protein 53 Brugada syndrome 53 holoprosencephaly 53 glycogen synthase kinase 53 JAK mutations 53 presenilin 53 FHIT 53 chromosome #p#.# 53 SHANK3 gene 53 choroidal neovascularization CNV 53 multisystem disease 53 TCF4 53 neovascularisation 53 normal karyotype 53 supratentorial 53 anterior pituitary 53 CFTR protein 53 medium chain acyl 53 antiphospholipid antibodies 53 cardiac fibrosis 53 neuro degenerative disease 53 TERT 53 microdeletions 53 5q 53 inherited neurodegenerative 53 proapoptotic 53 lymphoid 53 nonischemic 53 Wnt#b 53 infection progressive multifocal 53 MLL gene 53 PDE#A 53 da mage 53 genotoxic stress 53 leptin deficiency 53 IL #p# 53 5q chromosome 53 hyperparathyroidism 53 astrocytic 53 myelination 52 #q#.# [001] 52 hypomethylation 52 PALB2 52 Cockayne syndrome 52 fibrodysplasia ossificans progressiva 52 CYP #D# 52 Aß 52 aldehyde dehydrogenase 52 TSC1 52 beta globin gene 52 neurodegenerative disorder 52 TFIIH 52 fibrous dysplasia 52 Rb gene 52 IKK beta 52 amyloid deposits 52 HSF1 52 biomechanical integrity 52 factor HGF 52 inactivating mutations 52 pharmacodynamic biomarkers 52 interstitial pneumonitis 52 SLC#A# gene [001] 52 chromosomal rearrangement 52 MeCP2 gene 52 neuropathological 52 thyroid hormone deficiency 52 collagen VI 52 RUNX3 52 defective CFTR 52 nephrogenic fibrosing dermopathy 52 chromosomal translocations 52 epiphyseal 52 MYH9 gene 52 superoxide dismutase 52 unexplained mental retardation 52 non coding RNA 52 transcriptional machinery 52 lissencephaly 52 APOC3 52 NF2 52 nonsense mutation 52 #p#.# [001] 52 congenital anomalies 52 CMV infections 52 abnormal angiogenesis 52 polyposis 52 misregulation 52 cystic kidney 52 dystrophies 52 HLA B# 52 nonvascular 52 PCNSL 52 BRCA1 BRCA2 52 apoptosis pathway 52 unknown etiology 52 mesothelial cells 52 MYBPC3 52 hypoplastic 52 maternally inherited 52 hypopituitarism 51 genetic loci 51 apolipoprotein E gene 51 nonsense mutations 51 neoplastic 51 HMGCR 51 constitutively active 51 gene rearrangements 51 abnormal hemoglobin 51 rs# [004] 51 Bardet Biedl syndrome 51 leptin receptor 51 kidney insufficiency 51 neurofibroma 51 NR#A# gene 51 amyloid protein plaques 51 MC4R gene 51 microcephalin 51 BRCA2 gene 51 hepatic renal 51 periventricular 51 germline mutations 51 TOP2A 51 HMGA2 51 epigenetic alterations 51 Acidosis 51 vaccinia infection 51 F#del 51 inherited neurological disorder 51 connective tissue diseases 51 chromosomal defect 51 genetic syndromes 51 cytopathic 51 inherited retinal degeneration 51 arachnoiditis 51 DNA rearrangements 51 POMC neurons 51 CHD5 51 BDNF gene 51 mosaicism 51 MAPK pathway 51 shortened telomeres 51 WNK1 51 SMN2 51 chromosome #q#.# [002] 51 periodontal tissue 51 Amino acid 51 previously uncharacterized 51 HLA DRB1 * 51 neurologic deficits 51 inactive X chromosome 51 testicular tumors 51 dopamine D4 receptor 51 DICER1 gene 51 hamartomas 51 cytochrome c oxidase 51 IDH1 gene 51 chromosome rearrangements 51 huntingtin gene 51 substrate specificity 51 β cells 51 rs# [003] 51 Hip dysplasia 51 polymorphic ventricular tachycardia 51 Crouzon syndrome 51 kidney fibrosis 51 cyclophilin D 51 DiGeorge syndrome 51 myelomeningocele 51 Joubert syndrome 51 epigenetic markers 51 hydrops 51 TP# gene 51 Ehlers Danlos syndrome 51 retinal dystrophy 51 RPE# gene 51 chromosomal deletions 51 nonmelanoma 51 immunoreactivity 51 nerve palsy 50 superior mesenteric artery 50 adrenocortical cancer 50 mRNA transcripts 50 polyomavirus nephropathy 50 cerebral vasospasm 50 RCAN1 50 thoracic aortic aneurysm 50 GLI1 50 spontaneous mutation 50 mRNA expression 50 fatty degeneration 50 pre malignant lesions 50 Leber hereditary optic neuropathy 50 #p# [001] 50 transfusion syndrome 50 transgenic mice expressing 50 APOE4 50 mucosal immune responses 50 SORL1 50 neurosensory 50 abnormal prions 50 RNA splicing 50 levodopa induced 50 pneumonia septicemia 50 chromosome #p# [002] 50 promoter methylation 50 isotype 50 SLC#A# [001] 50 ZFN TM 50 Iron deficiency anemia 50 molecular abnormalities 50 Jhdm2a 50 TP# mutations 50 intracranial hemorrhage bleeding 50 EGFR gene 50 sickle hemoglobin 50 myeloproliferative disorder 50 thioredoxin 50 cortical dysplasia 50 CNTNAP2 50 hamartoma 50 incurable neurodegenerative disease 50 Corynebacterium 50 NQO1 50 myotonic muscular dystrophy 50 corneal opacity 50 spontaneous mutations 50 mitochondrial mutations 50 genetic defect 50 Genetic mutation 50 intergenic regions 50 uniparental 50 Sporadic CJD 50 corneal scarring 50 noncoding RNAs 50 gene p# 50 CREBBP 50 SNPs pronounced snips 50 neuro degenerative disorders 50 CDKN2A 50 metastatic lesions 50 ABCB1 gene 50 homocystinuria 50 retinitis pigmentosa RP 50 neuroblastoma tumor 50 FGFR2 gene 50 ribosomal DNA 50 NPM1 gene 50 invasive secretory carcinoma 50 histone H3 50 klotho 50 multiorgan 50 frataxin gene 50 RASSF1A 50 DNA glycosylase 49 IL #R 49 chromosomal imbalance 49 degenerative neurological disorder 49 TACI mutations 49 ERK2 49 neurologic abnormalities 49 cortical blindness 49 lesional 49 progressive degeneration 49 carboxy terminal 49 Anencephaly 49 synuclein 49 genes encoding 49 developmental abnormalities 49 c myb 49 HBx 49 Hemolytic uremic syndrome 49 miRNA genes 49 ABCA1 gene 49 neurological sequelae 49 paralysis blindness 49 muscle degeneration 49 cardiovascular malformations 49 leukoencephalopathy 49 microRNA molecules 49 recessive mutation 49 prematurity ROP 49 microvessels 49 globin 49 obliterative bronchiolitis 49 KLF4 49 renal scarring 49 vasogenic edema 49 OCT4 49 allograft rejection 49 aortic rupture 49 G6PD deficiency 49 recessive genetic 49 sequence homology 49 beta thalassemia 49 ischemic mitral regurgitation 49 E4 variant 49 connective tissue disorders 49 skeletal fluorosis 49 receptor gene 49 cervical spinal cord 49 retinal dysfunction 49 iNOS 49 IKZF1 49 nonhematologic adverse reactions 49 alpha helix 49 pilocytic astrocytomas 49 polyglutamine 49 Benign tumors 49 acute aortic dissection 49 chromosome abnormality 49 FOXP3 49 breast carcinomas 49 transiently transfected 49 Folic acid deficiency 49 chromosome #q 49 alternatively spliced 49 aberrant methylation 49 Leber congenital amaurosis LCA 49 intraoperative complications 49 Lesch Nyhan syndrome 49 Fanconi anemia 49 gene amplification 49 benign positional vertigo 49 dystrophin 49 palates congenital 49 amino acid substitution 49 bone deformities 49 Lupus nephritis 49 abnormalities 49 valvular heart disease 49 pAkt 49 histone demethylase 49 leukoencephalopathy PML 49 homozygote 49 anatomical abnormalities 49 somatic mutations 49 MTHFR gene 49 bile acid metabolism 49 coagulation parameters 49 desmosomes 49 ARVD 49 vascular occlusion 49 chromosome aberrations 49 short hairpin RNAs 49 CNTNAP2 gene 49 gene loci 49 Leber congenital amaurosis 49 APOA5 49 circulating endothelial cells 49 chromosome #q# [002] 49 morphological abnormalities 49 bcl 2 49 frameshift mutation 49 micrometastasis 49 Bcl XL 49 ataxin 49 aciduria 48 spontaneous miscarriages 48 proline 48 DiGeorge Syndrome 48 Idiopathic pulmonary fibrosis IPF 48 mPGES 1 48 intestinal biopsy 48 lymphatic vasculature 48 cervical degenerative disc 48 breast cancer genes BRCA1 48 chromosomal disorder 48 nephrosis 48 intronic 48 Hirschsprung disease 48 dysplastic lesions 48 perfusion abnormalities 48 gene deletions 48 Raynaud disease 48 somatic mutation 48 chromosomal anomalies 48 DISC1 gene 48 cochlear nerve 48 skeletal malformations 48 uremia 48 metalloproteases 48 Aplastic anemia 48 chromosome #q# [001] 48 p tau 48 radiculopathy 48 Sp1 48 degenerative disorder 48 Folate deficiency 48 EBNA1 48 Pulmonary fibrosis 48 intestinal mucosa 48 mitochondrial proteins 48 spinal muscular atrophy SMA 48 gene encoding 48 PrP 48 RNA polymerases 48 Intussusception 48 Lewy bodies 48 PCSK9 gene 48 lamin 48 hypertrophic cardiomyopathy HCM 48 neural tube 48 postoperative delirium 48 SOCS3 48 paralogs 48 renal tubular acidosis 48 congenital deafness 48 polyhydramnios 48 downstream effectors 48 cystic lesions 48 Irs2 48 fetal chromosomal 48 androgen receptor gene 48 hepatic toxicity 48 FLT3 ITD 48 LPA gene 48 centromeric 48 Usher Syndrome 48 urinary blockage 48 beta amyloid proteins 48 ocular albinism 48 DLC1 48 auditory neuropathy 48 heterozygous 48 3' UTR 48 mesotheliomas 48 biochemical imbalances 48 missense 48 M. genitalium 48 phosphatases 48 intergenic 48 chromosome abnormalities 48 Plaque buildup 48 chromosomal DNA 48 Aortic stenosis 48 TGFBR1 48 SOD1 mutations 48 encephalitis inflammation 48 chromosomal alterations 47 peri implant 47 congenital disorders 47 anemias 47 atresia 47 azoospermia 47 histologic 47 pulmonary thromboembolism 47 hypermethylation 47 SLITRK1 47 granule cells 47 neurologic sequelae 47 number variations CNVs 47 prion gene 47 mRNA sequences 47 retinoid cycle 47 tumor suppressor PTEN 47 Nephrogenic Systemic Fibrosis NSF 47 congenital scoliosis 47 polyadenylation 47 Chromosomal 47 HPRT gene 47 chick embryos 47 biogenesis 47 PALB2 gene 47 HERV K 47 subaortic stenosis 47 Foxp2 47 ribosomal RNA 47 multiprotein complex 47 splice junctions 47 Epigenetics refers 47 structural rearrangements 47 polyps growths 47 genetic alterations 47 cartilage defects 47 galactosemia 47 GDNF gene 47 Vascular dementia 47 undiagnosed celiac disease 47 fetal malformations 47 behavioral disturbances 47 variant allele 47 brain malformation 47 GLUT1 47 defects CHDs 47 bullous pemphigoid 47 NHEJ 47 Degenerative disc disease 47 Reye syndrome rare 47 structural abnormalities 47 adenoma 47 Bcl 47 epigenetic changes 47 indels 47 thoracic aortic disease 47 diffuse intrinsic pontine glioma 47 Lkb1 47 micro RNAs 47 M. capricolum 47 autoimmune hemolytic anemia 47 clade C 47 DNA methyltransferase 47 recessive trait 47 hippocampal atrophy 47 #p# [003] 47 tardive dyskinesia TD 47 post translational modifications 47 meningitis sepsis 47 Chiari malformation 47 ectopia 47 renal agenesis 47 degenerative retinal disease 47 mitral stenosis 47 CYP#C# * 47 phylogenetic analyzes 47 Malignant glioma 47 genomic deletions 47 polymorphisms 47 extracellular domains 47 hepatic enzymes 47 cognitively normal 47 chromosomal abnormalities 47 cerebral vascular disease 47 esophageal atresia 47 cardiac tamponade 47 benign polyps 47 CTL epitopes 47 retinal haemorrhages 47 S. pombe 47 lung cancer NSCLC 47 unmethylated 47 idiopathic epilepsy 47 SORL1 gene 46 muscular degeneration 46 chromatin proteins 46 Pulmonary hypertension 46 ventricular septum 46 Vitamin B# deficiency 46 number variation CNV 46 histologic examination 46 MYH# 46 SPINK1 46 DSBs 46 interrupted aortic arch 46 genes BRCA1 46 inheritable genetic 46 CCL#L# 46 coding exons 46 enzyme deficiency 46 spondylolysis 46 congenital abnormality 46 Ebstein anomaly 46 rRNA 46 carotid artery dissection 46 neuropsychological impairments 46 type II pneumocytes 46 Alleles 46 Plain radiographs 46 Critical limb ischemia 46 placental tissues 46 corneal edema 46 number variants CNVs 46 mutant alleles 46 microcirculatory improvement helping 46 Malignant mesothelioma 46 microRNA expression 46 nonmalignant 46 luminal 46 reproductive abnormalities 46 Arabidopsis genome 46 encode proteins 46 meiotic recombination 46 GlcNAc 46 Lumbar spinal stenosis 46 neural tube defect 46 autosomal 46 congenital malformations 46 perineural invasion 46 Crouzon Syndrome 46 Neural tube defects 46 antigenicity 46 deep vein thromboses 46 blood clotting disorder 46 H#Y 46 thrombi 46 L5 S1 46 gingival recession 46 allelic 46 blindness paralysis 46 craniofacial deformities 46 homologues 46 dysmorphic features 46 inherited predisposition 46 heterochromatin 46 corneal inflammation 46 mental retardation blindness 46 enterovirus infection 46 unprovoked seizures 46 capillary leakage 46 cell sarcoma 46 immunodominant 46 abruption 46 degenerative neurological disease 46 familial aggregation 46 stenosis narrowing 46 XMRV infection 46 meniscal tears 46 bacterial endocarditis 46 defective cilia 46 congenital cataract 46 thyroid dysfunction 46 gene duplications 46 lumbosacral spine 46 Alu elements 46 Torsades de Pointes 46 congenital disorder 46 bicuspid valve 45 F#del mutation 45 ADH1B * 45 defective gene 45 bladder tumors 45 pseudoaneurysm 45 folic acid deficiency 45 osteochondromas 45 behavioral abnormalities 45 NPM1 mutations 45 Ph chromosome 45 miR #b [001] 45 terminal ileum 45 telomeric 45 viral proteins 45 pulmonary valves 45 posttranslational 45 PBMCs 45 chromosome #p# [001] 45 CHDs 45 gene mutations 45 PTP1B 45 dopamine synthesis 45 selective agonists 45 3'UTR 45 mutation 45 anoxic brain injury 45 vein thrombosis 45 Postoperative complications 45 cytosolic 45 exceptionally broadly neutralizing 45 At#g# 45 histiocytosis 45 genomic instability 45 Down syndrome chromosomal disorder 45 Histologic 45 cardioembolic stroke 45 symptomatic pulmonary embolism 45 heterozygosity 45 LMNA gene 45 mutations 45 alternative splicing 45 ganglion cysts 45 hereditary disorder 45 tricuspid valve 45 airway blockage 45 endogenous retroviruses 45 histopathological 45 limb deformities 45 uracil 45 renal biopsy 45 aortic valve stenosis 45 bowel perforations 45 microRNAs miRNAs 45 Acute pancreatitis 45 morphologic 45 alleles 45 cytoplasmic tail 45 #q# [002] 45 filaggrin gene 45 prenatally diagnosed 45 nucleotide sequence 45 micro RNA 45 heterochromatic 45 epigenetic modifications 45 electrical conduction 45 MiRNAs 45 Cytogenetic 45 DNMT3A 45 secondary bacterial pneumonia 45 Pten gene 45 guinea pigs lubiprostone 45 tricuspid atresia 45 DNA polymerases 45 Ehlers Danlos Syndrome 45 T1 weighted images 45 mitochondrial defects 45 Churg Strauss syndrome 45 blindness deafness 45 perfusion defects 45 premutation 45 Lemierre syndrome 45 persistent pulmonary hypertension 45 osteochondritis dissecans 45 tumor suppressor genes 45 etiologic 45 klotho gene 45 Rh incompatibility 44 chimeric mice 44 genomic variants 44 unmeasured confounding 44 mitochondrial DNA mtDNA 44 CCR5 gene 44 C#Y mutation 44 urethral stricture 44 MC1R gene 44 segmental duplications 44 congenital hypothyroidism 44 glutamate signaling 44 Neural tube 44 amniotic fluid embolism 44 Anaphylactic reactions 44 genomic rearrangements 44 colonic polyps 44 serum BDNF 44 cis regulatory 44 epidural abscess 44 dopaminergic cells 44 systemic toxicity 44 Goldenhar syndrome 44 cardiac valvulopathy 44 biliary obstruction 44 Her2 gene 44 Osr2 44 hemolytic disease 44 GFP gene 44 thrombotic complications 44 tricuspid regurgitation 44 bone deformity 44 optic nerve hypoplasia 44 valine 44 μ opioid receptor 44 TGF beta signaling 44 atrial arrhythmias 44 hereditary disorders 44 respiratory insufficiency 44 epithelial markers 44 phonic tics 44 peritoneal mesothelioma 44 Cleft palate 44 subdural haemorrhage 44 oral hypoglycemic agents 44 postoperative complication 44 liver enlargement hepatomegaly 44 Bifidobacterium infantis # 44 lumbosacral 44 ectasia 44 retinal detachments 44 polymorphism 44 interfering RNAs siRNAs 44 hormonal abnormalities 44 D#N 44 muscle protein dystrophin 44 chromosomal rearrangements 44 chromatid 44 neurological complications 44 Nrf2 gene 44 endocasts 44 chromosome translocations 44 abdominal aortic 44 untranslated regions 44 globin genes 44 ORFs 44 atrioventricular 44 clinicopathologic 44 urologic diseases 44 descending thoracic aorta 44 genetic recombination 44 malignant polyps 44 arterial occlusion 44 Aß peptide 44 long QT syndrome 44 pseudogene 44 oral clefts 44 Aortic valve 44 chordate 44 tracheal stenosis 44 NSF NFD 44 acetylation 44 chromosomal abnormality 44 acetyl groups 44 gastric antrum 44 perioperative complications 44 ncRNAs 44 quasispecies 44 atypical femur fractures 44 FOXP2 gene 44 cerebral ischemia 44 cytosine 44 myeloid cells 44 microtrauma 44 insertions deletions 44 PGRN 44 BRCA1 gene 44 CETP VV 44 insulin deficiency 44 MC4R 44 monozygotic twins 44 fungus Fusarium 43 noncoding 43 congenital diaphragmatic hernia 43 syncope fainting 43 aneurysm rupture 43 Nf1 gene 43 genetic abnormality 43 K ras gene 43 esotropia 43 HAR1 43 K#N 43 cytosine methylation 43 Down syndrome spina bifida 43 mitral valve regurgitation 43 congential 43 incisional hernia 43 red scaly skin 43 abnormal growths 43 vascular abnormalities 43 anatomic abnormalities 43 oxidative lesions 43 bowel perforation 43 congenital cardiac 43 rebleeding 43 chromosomal defects 43 CHARGE syndrome 43 outflow tract 43 mitochondrial gene 43 malperfusion 43 receptor subunits 43 thrombotic thrombocytopenic purpura TTP 43 congenital defects 43 polydactyly 43 exons 43 cDNAs 43 HLHS 43 Exclusion criteria 43 pyloric stenosis 43 Bankart lesion 43 combined immunodeficiency SCID 43 cerebral anoxia 43 ACE2 gene 43 vertebral subluxations 43 diseases chronic granulomatous 43 HER2 gene 43 deformed limbs 43 cerebellar ataxia