Related by context. All words. (Click for frequent words.) 66 Hutchinson Gilford progeria 65 #q#.# [001] 64 microdeletion 64 de novo mutations 64 #q#.# deletion syndrome 63 autosomal recessive 63 nonhereditary 63 Li Fraumeni syndrome 62 Lafora disease 62 inherited mutations 62 chromosome abnormality 62 #p#.# [001] 62 paraneoplastic 61 monogenic 61 holoprosencephaly 61 #p# [001] 61 JAK mutations 61 genetic syndromes 61 autosomal dominant 61 velo cardio facial 61 autosomal dominant disorder 61 rare chromosomal disorder 61 chromosomal rearrangements 61 neurodevelopment disorder 60 neurodevelopmental disorder 60 missense mutations 60 McCune Albright 60 Medulloblastoma 60 predisposing factor 60 MYH9 gene 60 chromosomal anomalies 60 familial clustering 60 Severe Combined Immunodeficiency 60 #p#.# [002] 60 VCFS 60 #q# [001] 60 Genetic predisposition 60 MECP2 gene 59 chromosome #q#.# [001] 59 CDH1 59 autosomal dominant inheritance 59 Angelman syndrome 59 von Hippel Lindau 59 Hashimoto thyroiditis 59 congenital adrenal hyperplasia CAH 59 paraganglioma 59 Beckwith Wiedemann syndrome 59 chromosomal anomaly 59 monozygotic twins 59 congenital disorders 59 autosomal recessive disorder 59 IgA deficiency 59 neuropsychiatric disorder 59 inherited predisposition 58 pyloric stenosis 58 Kufs disease 58 autoinflammatory diseases 58 primitive neuroectodermal tumors 58 Hirschsprung disease 58 dominantly inherited 58 hydrops 58 MELAS 58 maternally inherited 58 Wolf Hirschhorn 58 cerebellar hypoplasia 58 #q#.# [002] 58 extramedullary 58 childhood disintegrative disorder 58 germline mutations 58 MYH9 58 dyskeratosis congenita 58 transfusion syndrome 58 recessive genetic 58 Dravet syndrome 58 neuroblastomas 58 CNVs 58 Kleine Levin 58 Aicardi syndrome 58 penetrance 58 MeCP2 gene 58 generalized epilepsy 58 cri du chat 58 Genetic variants 58 proband 58 polygenic 58 ependymoma 58 chromosomal rearrangement 58 TCF#L# gene 58 chromosome #q 58 progressive neurodegenerative disorder 58 vascular Ehlers Danlos 58 Dwarfism 58 monozygotic twin 57 aneuploidies 57 Von Hippel Lindau 57 Klinefelter syndrome 57 epilepsies 57 gastric carcinoma 57 Bardet Biedl syndrome 57 genetic loci 57 Von Willebrand disease 57 MLL gene 57 chromosomal disorder 57 recessive trait 57 mosaicism 57 autistic regression 57 FASPS 57 congenital deafness 57 DiGeorge Syndrome 57 underlying pathophysiology 57 superior mesenteric artery 57 post transplant lymphoproliferative 57 mitochondrial disorders 57 hamartomas 57 #q# deletion 57 lymphocytic 57 Proteus Syndrome 57 dysgenesis 57 Spinal muscular atrophy 57 hereditary predisposition 57 susceptibility locus 57 antiphospholipid syndrome 57 Wilms tumor 57 neurofibromatosis type 57 microdeletions 57 familial pancreatic cancer 57 astrocytomas 57 HGPS 57 Apert syndrome 57 undiagnosed celiac disease 57 situs inversus 57 hyperinsulinemia 56 MC4R gene 56 chromosome #q# [002] 56 susceptibility gene 56 Neurofibromatosis type 56 genetic abnormality 56 IL#R 56 Bardet Biedl Syndrome 56 apolipoprotein E gene 56 mitochondrial mutations 56 Autistic Disorder 56 NF1 56 genes predisposing 56 Spina bifida 56 MELAS syndrome 56 Tay Sachs genetic 56 neurofibroma 56 Alport syndrome 56 ADPKD 56 BARD1 56 autosomal 56 autosomal recessive disease 56 neuro developmental disorder 56 chromosome #q#.# deletion 56 MSH2 56 Foetal alcohol 56 granulosa cell 56 nucleoli 56 G6PD deficiency 56 fatal neurodegenerative disorder 56 ORMDL3 56 NR#A# 56 anencephaly 56 Intussusception 56 Fatty liver 56 PTPN# 56 microcephalin 56 NPHP 56 clinically heterogeneous 56 Dysplasia 56 Joubert syndrome 56 neurofibromas 56 VHL gene 56 Brugada syndrome 56 MLH1 56 Crouzon Syndrome 56 Tay Sachs Disease 56 MLL2 56 Proteus syndrome 56 Vitamin B# deficiency 56 Childhood Disorder 56 LIS1 56 STAT4 56 phthalate syndrome 56 LRRK2 gene 56 comorbid anxiety 56 SHANK3 gene 56 KCNH2 56 gene APOE4 56 developmental abnormalities 56 myelogenous leukemia 56 inherited neurological disorder 56 epigenetic modification 56 GPC5 56 INF2 56 chronic obstructive airway 56 chromosomal instability 56 chromosome #p#.# 56 DNA methylation patterns 56 achondroplasia 56 puerperal psychosis 56 spongiform encephalopathies 56 CALHM1 56 myeloproliferative neoplasms 55 autosomal recessive genetic 55 spontaneous mutations 55 Chronic lymphocytic leukemia 55 CNTNAP2 55 Hutchinson Gilford Progeria 55 Endometrial cancer 55 primary ciliary dyskinesia 55 internalizing disorders 55 Hurler syndrome 55 polydactylism 55 Rb gene 55 FGFR2 gene 55 epigenetic changes 55 teratoma 55 HNPCC 55 embryonal rhabdomyosarcoma 55 mammary stem cells 55 Leber congenital amaurosis 55 Heredity 55 imperfecta 55 IRF6 55 pseudotumor cerebri 55 skeletal dysplasia 55 fibrodysplasia ossificans progressiva 55 Fragile X gene 55 persistent pulmonary hypertension 55 epigenetic alterations 55 susceptibility genes 55 maternally transmitted 55 highly heritable 55 Marfan syndrome connective tissue 55 medium chain acyl 55 hypercoagulable 55 TP# mutation 55 karyotypes 55 hyperinsulinism 55 leptin deficiency 55 recessive inheritance 55 ependymomas 55 chromosomal deletions 55 chromosomal alterations 55 CHD7 55 Mendelian disorders 55 familial polyposis 55 inappropriate antidiuretic hormone SIADH 55 genomic imprinting 55 enterocolitis 55 neurodevelopmental disorders 55 testicular germ cell 55 chronic myeloid 55 ANCA associated 55 susceptibility loci 55 Henoch purpura 55 SLC#A# gene [001] 55 severe congenital neutropenia 55 myositis 55 familial aggregation 55 Chromosome 55 cystic fibrosis Duchenne muscular 55 MEF2A 55 galactosemia 55 monogenic disorders 55 Niemann Pick disease 55 apoE4 55 euthymic patients 55 gene MECP2 55 WAGR syndrome 55 hereditary hemochromatosis 55 APOL1 55 HLA DRB1 55 endogenous retroviruses 55 chromosomal disorders 55 Leukemias 55 Kabuki syndrome 55 hypertrichosis 55 breast cancer subtypes 55 FMR1 55 beta thalassemia 55 mycosis fungoides 55 hepatoblastoma 55 Fetal alcohol 55 microchimerism 55 twin transfusion 55 metabolic abnormality 55 Sudden infant 55 cortical dysplasia 55 neurological disorder affecting 55 carbohydrate intolerance 55 sporadic ALS 55 pathophysiologic 55 G#S mutation 55 carcinoid tumor 54 thyroid hormone deficiency 54 ASD autism spectrum 54 synaptogenesis 54 Chromosomal 54 CHARGE syndrome 54 dopamine transporter gene 54 HER2 positivity 54 FXTAS 54 polycystic ovarian syndrome PCOS 54 essential thrombocythemia 54 mitochondrial dysfunction 54 osteosarcomas 54 Coeliac disease 54 autoinflammatory 54 radial glia 54 Pervasive Developmental Disorder 54 hereditary nonpolyposis colorectal cancer 54 hereditary hemorrhagic telangiectasia 54 Chiari malformation 54 multisystem disease 54 5 HTTLPR 54 clefting 54 microRNA expression 54 Tay Sachs disease 54 static encephalopathy 54 mental retardation epilepsy 54 haemochromatosis 54 neurological abnormalities 54 hereditary deafness 54 autistic enterocolitis 54 Langerhans cell histiocytosis 54 CYP#C# gene 54 genomic deletions 54 aetiological 54 chromosome abnormalities 54 PNET 54 aneuploidy 54 familial adenomatous polyposis FAP 54 phenotypic expression 54 dopamine D4 receptor 54 Sanfilippo Syndrome 54 ectodermal dysplasia 54 Reflex sympathetic dystrophy 54 lysosomal storage diseases 54 BRCA1 BRCA2 54 osteopetrosis 54 etiological 54 multifactorial 54 inherited neurodegenerative 54 klotho 54 supratentorial 54 KRAS oncogene 54 ARVD 54 Male pattern baldness 54 CYP#D# gene 54 prenatally diagnosed 54 CHEK2 54 Inflammatory bowel disease 54 granulomatous 54 adenomyosis 54 T1DM 54 neonatal respiratory distress 54 GISTs 54 Prox1 54 affective psychosis 54 Sudden Unexpected Death 54 Raynaud syndrome 54 medulloblastomas 54 myelomeningocele 54 lymphangioleiomyomatosis LAM 54 dissociative disorders 54 juvenile myelomonocytic leukemia 54 NF2 54 myeloproliferative 54 Polycystic Ovarian Syndrome PCOS 54 Atopic dermatitis 54 Polycystic ovary syndrome 54 leukaemias 54 SLITRK1 54 SHANK3 54 circulating endothelial cells 54 recessive mutation 54 chromosomal abnormality 54 somatic mutations 54 biochemical imbalance 54 neuronal dysfunction 54 oligodendrogliomas 54 Fanconi Anemia 54 polymorphic ventricular tachycardia 54 neoplasm 54 hypogonadotropic hypogonadism 54 bronchopulmonary dysplasia 54 EoE 54 COMT gene 54 familial ALS 54 chromosomal translocations 54 IKZF1 54 retinoblastoma Rb 54 chromosomal defect 54 LPA gene 54 eosinophilic esophagitis 54 diathesis 54 ALK gene 54 LRP5 54 clinicopathological 54 fronto temporal dementia 54 homozygosity 54 Wernicke Korsakoff syndrome 54 #p# [003] 54 congenital insensitivity 54 Rubinstein Taybi syndrome 54 blastoma 54 DNA rearrangements 54 hormonal disorder 54 congenital adrenal hyperplasia 54 Mitochondrial dysfunction 54 heritable 54 polyglutamine 54 ABCB1 gene 54 congenital anomalies 54 DISC1 gene 54 comorbid disorders 54 genetic polymorphism 54 PANDAS 54 testicular tumors 54 Genetic mutations 54 inherited genetic mutations 54 Sjögren syndrome 54 mutant huntingtin protein 54 lysosomal storage disease 54 spontaneous mutation 54 metabolic disturbances 54 lissencephaly 54 Meckel Gruber 54 familial adenomatous polyposis 54 sporadic Creutzfeldt Jakob 54 Cognitive impairment 53 polycystic kidneys 53 hypoplasia 53 DISC1 53 thrombophilia 53 chromosome #q#.# [002] 53 FMR1 gene 53 HLA B# 53 Leber congenital amaurosis LCA 53 androgen excess 53 gene rearrangements 53 Loeys Dietz 53 enteropathy 53 fibrous dysplasia 53 incurable genetic 53 idiopathic pulmonary 53 ADAM# 53 paragangliomas 53 progressive degenerative neurological 53 skeletal abnormalities 53 Polycystic kidney disease 53 serous ovarian cancer 53 p# mutation 53 spinocerebellar ataxia type 53 immunodeficiencies 53 Porphyria 53 hyperemesis gravidarum 53 Klinefelter Syndrome 53 clinicopathologic 53 BRIP1 53 spinocerebellar ataxia 53 Sudden Unexplained Death 53 multisystem disorder 53 Premature Ovarian Failure 53 HMGA2 53 caveolin 53 karyotype 53 Congenital Adrenal Hyperplasia 53 DQB1 * 53 Chronic constipation 53 basal cell nevus syndrome 53 hemophagocytic lymphohistiocytosis 53 gastrointestinal dysfunction 53 Beta thalassemia 53 missense mutation 53 stress cardiomyopathy 53 MC1R 53 Wernicke encephalopathy 53 Sanfilippo syndrome 53 dementia praecox 53 juvenile idiopathic arthritis JIA 53 microscopic colitis 53 spastic diplegia 53 Oxidative stress 53 Morquio syndrome 53 immune reconstitution inflammatory 53 eosinophilic 53 Tuberous sclerosis 53 5q 53 causative genes 53 Rh incompatibility 53 polyploidy 53 muscular dystrophy cystic fibrosis 53 embryonal 53 fatal neuromuscular disorder 53 chromosomal aberrations 53 MALT lymphoma 53 mtDNA mutations 53 de ath 53 progressive neurodegenerative 53 Hereditary angioedema 53 familial hypercholesterolemia 53 Hutchinson Gilford Progeria Syndrome 53 associated tremor ataxia 53 osteochondroma 53 somatoform disorders 53 sCJD 53 Diamond Blackfan anemia 53 immunodeficiency disorder 53 SLC#A# [001] 53 CNTNAP2 gene 53 non coding RNA 53 monoclonal gammopathy 53 hormonal abnormalities 53 Neurofibromatosis Type 53 dopamine receptor gene 53 omphalocele 53 chronicity 53 ataxias 53 myopathies 53 Folate deficiency 53 APOE e4 53 narcolepsy cataplexy 53 #q# deletion syndrome 53 C#Y 53 chronic granulomatous disease 53 microcephaly 53 autonomic dysfunction 53 Cryptococcus neoformans 53 tonic clonic 53 dizygotic twins 53 GH deficiency 53 PCOD 53 Cowden syndrome 53 Wilms Tumor 53 familial hypercholesterolemia FH 53 Glioma 53 pheochromocytomas 53 MTHFR 53 non syndromic 53 progressive multifocal PML 53 leptin receptor 53 ccRCC 53 Binge eating 53 MCADD 53 congenital anomaly 53 complement inhibitor eculizumab 53 ADAMTS# 53 genomic rearrangements 53 hyperplastic 53 MAPK pathway 53 CYP#E# gene 53 malignant brain 53 WDR# 53 hyper IgE syndrome 53 TP# gene 53 idiopathic epilepsy 53 polyhydramnios 53 hypoactive 53 Irritable bowel syndrome IBS 53 Pelizaeus Merzbacher disease 53 atypical hemolytic uremic syndrome 53 Ankylosing spondylitis 53 HLA identical 53 alveolar rhabdomyosarcoma 53 choriocarcinoma 53 aldehyde dehydrogenase 53 progeria rare 53 PARP inhibition 53 hypertrophic cardiomyopathy HCM 53 dysbindin 53 molecular abnormalities 53 SIDS Sudden Infant Death 53 Shy Drager syndrome 53 genetically inherited 53 polyglutamine diseases 53 chromosome #p# [001] 53 CCR5 delta# 53 thyroid carcinoma 53 chromosome rearrangements 53 BRAF V#E 53 polydactyly 53 leiomyoma 53 antenatal depression 53 congenital toxoplasmosis 53 histiocytosis 53 intraventricular hemorrhage 53 functional polymorphism 53 methylation patterns 53 tuberous sclerosis complex 52 renal fibrosis 52 sarcomatoid 52 sub syndromal 52 tricuspid atresia 52 cryptogenic 52 Leber hereditary optic neuropathy 52 asplenia 52 autoimmune hemolytic anemia 52 systemic mastocytosis 52 Genetic mutation 52 normal karyotype 52 fibromatosis 52 Menkes disease 52 metaplasia 52 hemoglobinopathies 52 Smad3 52 syndromes 52 Gluten intolerance 52 lymphatic vasculature 52 urolithiasis 52 progressive neurodegenerative disorders 52 FGFs 52 PCNSL 52 neonatal lupus 52 chronic autoimmune disorder 52 schwannoma 52 cerebri 52 behavioral disinhibition 52 underactive thyroid gland 52 thyrotoxicosis 52 pathogenic mutations 52 dysmorphic features 52 mitochondrial DNA mtDNA 52 polymyalgia rheumatica 52 Androgenetic alopecia 52 breast carcinomas 52 epigenetic modifications 52 PTEN gene 52 breast carcinoma 52 SLC#A# [002] 52 KIBRA 52 Dilated cardiomyopathy 52 Loeys Dietz syndrome 52 ENPP1 52 infantile hemangioma 52 diffuse pontine glioma 52 Mitochondrial diseases 52 ApoE gene 52 autoimmune pancreatitis 52 STK# gene 52 hay fever allergic rhinitis 52 autosomal dominant polycystic kidney 52 fibrodysplasia ossificans progressiva FOP 52 nonalcoholic steatohepatitis NASH 52 Alopecia areata 52 polycystic ovary syndrome 52 DRD4 52 neurobiological disorder 52 Smith Lemli Opitz 52 p# mutations 52 BRCA1 mutation carriers 52 prepubertal 52 nondemented 52 retinal dysfunction 52 somatic mutation 52 arterial thickening 52 monozygotic 52 hirsutism 52 Arrhythmogenic Right Ventricular Cardiomyopathy 52 Becker muscular dystrophy 52 Progeria 52 congenital hypothyroidism 52 cytogenetic abnormalities 52 receptor gene 52 Polycystic ovarian syndrome 52 sensorineural hearing loss 52 thyroid dysfunction 52 IUGR 52 CDH# 52 pre eclamptic 52 Fanconi anemia 52 Genetic variation 52 APOE ε4 52 Patau syndrome 52 recessively inherited 52 HLA DQ2 52 neuroendocrine 52 K ras mutations 52 adenocarcinomas 52 Osteogenesis imperfecta 52 Polycystic Ovary Syndrome 52 Bacterial vaginosis 52 incurable neurodegenerative disease 52 Sudden Arrhythmic Death 52 lung adenocarcinoma 52 pheochromocytoma 52 acanthosis nigricans 52 lysosomal diseases 52 alexithymia 52 aetiology 52 cystic kidney 52 Retinoblastoma 52 genomic instability 52 bicuspid valve 52 Celiac sprue 52 Acute lymphoblastic leukemia 52 sirenomelia 52 MECP2 52 etiologic 52 Hurler Syndrome 52 exocrine 52 1 diabetes T1D 52 MPGN 52 breast cancer genes BRCA1 52 PALB2 52 Insulin resistance 52 nongenetic 52 fatal neurodegenerative 52 cholestasis 52 SCA5 52 Hypoplastic Left Heart 52 Treacher Collins 52 precocious puberty 52 autism Asperger 52 chorioamnionitis 52 KIF6 gene 52 homocystinuria 52 Chronic fatigue 52 folate metabolism 52 astrocytoma 52 APOE4 52 airway hyperresponsiveness 52 NPM1 gene 52 aneuploid 52 hypothalamic pituitary adrenal axis 52 lipodystrophy syndrome 52 medulloblastoma tumors 52 folate deficiency 52 IGF1 52 Polycystic ovary syndrome PCOS 52 untreated celiac disease 52 Systemic lupus erythematosus 52 facioscapulohumeral muscular dystrophy 52 motor neuron degeneration 52 airway remodeling 52 recessive dystrophic epidermolysis bullosa 52 filaggrin 52 Dental caries 52 Postnatal depression 52 Pervasive Developmental Disorders 52 Peritoneal mesothelioma 52 endocannabinoid signaling 52 myofascial pain syndrome 52 deafness neurological 52 lichen planus 52 Aortic stenosis 52 infertility miscarriages 52 biliary atresia 52 schizotypal 52 modifier genes 52 Phenylketonuria PKU 52 underdiagnosis 52 Fragile X Syndrome 52 MGUS 52 allelic variants 52 Hypertrophic cardiomyopathy 52 myalgic encephalomyelitis ME 52 huntingtin gene 52 endophenotypes 52 insulin resistance syndrome 52 Alternative splicing 52 chromosomal defects 52 diffuse intrinsic pontine glioma 52 gene APOE 52 causative gene 52 congenital muscular dystrophies 52 Obsessive compulsive disorder 52 Retinitis pigmentosa 52 BMPR2 52 Wiskott Aldrich syndrome 52 neural tube defect 52 G6PD 52 postural orthostatic tachycardia 52 congenital scoliosis 52 nephrosis 52 hypokalemia hypomagnesemia 52 Brugada Syndrome 52 endocrine disorder 52 Heritability 52 microRNA molecules 52 unknown etiology 52 Bronchiolitis 52 Muscular dystrophy 52 congenital CMV 52 Sonic Hedgehog 52 hyperemesis 52 lobular breast cancer 52 Prader Willi syndrome 52 asperger syndrome 52 disabling neurological 52 heterotaxy 52 periventricular 52 mitochondrial gene 52 miRNA genes 52 ataxia telangiectasia 52 UGT#B# 52 biliary atresia rare 52 pathogenetic 52 Vascular dementia 52 Rh factor 52 epigenetic regulation 52 medial tibial stress 52 FSGS 52 Li Fraumeni 51 vascular dysfunction 51 dysmorphic 51 Crouzon syndrome 51 C. neoformans 51 acute myeloid 51 DiGeorge syndrome 51 Diabetic neuropathy 51 Major depressive disorder 51 inherited retinal degeneration 51 neuritic 51 ectopic 51 Maternal obesity 51 fat malabsorption 51 Morquio 51 DRD2 gene 51 rhabdomyosarcoma 51 medulloblastoma 51 idiopathic PAH 51 heterozygosity 51 placental insufficiency 51 HELLP 51 molar pregnancy 51 dysautonomia 51 endocrine tumors 51 congenital diaphragmatic hernia 51 somatoform disorder 51 C1q 51 hemolytic disease 51 renal carcinoma 51 BRAF gene 51 motor neuron diseases 51 Oppositional Defiant Disorder 51 Persistent Sexual Arousal 51 CYP#A# gene 51 FOXP2 gene 51 Magnesium deficiency 51 GBA mutations 51 Neuregulin 1 51 Clusterin 51 demyelination 51 IRAK1 51 HbF 51 PON1 51 tics involuntary 51 Hip dysplasia 51 cerebellar 51 leukoencephalopathy 51 mental retardation syndromes 51 APOE genotype 51 genetic imprinting 51 abnormal chromosome 51 primary biliary cirrhosis 51 RET PTC rearrangements 51 Autoimmune disorders 51 amyloid cascade 51 meiotic recombination 51 MYBPC3 51 premutation 51 hippocampal function 51 utero exposure 51 CREBBP 51 acute lymphoblastic 51 LMNA gene 51 Lesch Nyhan syndrome 51 recessive gene 51 neural crest 51 chordate 51 recurrent miscarriage 51 Radiographic findings 51 Empty nest 51 autoimmune thyroid 51 Y chromosomal 51 MCAD deficiency 51 Holoprosencephaly 51 Notch signaling 51 BCL#A 51 ABCB1 51 induced cardiomyopathy 51 gestational diabetes mellitus GDM 51 spastic paraplegia 51 TMPRSS2 ERG fusion 51 Chronic ITP 51 UGT#A# * 51 #q# [002] 51 maturational 51 SCN5A 51 amnestic 51 allergic sensitization 51 obese postmenopausal 51 Churg Strauss syndrome 51 mitochondrial diseases 51 hyperparathyroidism 51 lymphoproliferative disorder 51 MYCN amplification 51 hypermethylation 51 Fragile X mental retardation 51 ceroid lipofuscinosis NCL 51 NF1 gene 51 causative mutation 51 Hereditary angioedema HAE 51 congenital hemophilia 51 Alleles 51 TTR amyloidosis 51 systemic lupus erythematosus SLE 51 thrombocytosis 51 neurodegenerative disorder 51 fructose intolerance 51 Cockayne syndrome 51 Myotonic dystrophy 51 hypotonia 51 pilocytic astrocytomas 51 neuroligins 51 segmental duplications 51 autoimmune thyroiditis 51 Apolipoprotein E 51 familial hypercholesterolaemia FH 51 mutated gene 51 acute lymphoid leukemia 51 myoclonic epilepsy 51 syndrome FAS 51 ADH1B * 51 Lichen planus 51 savant syndrome 51 Epstein Barr Virus 51 Osteopenia 51 schizophreniform disorder 51 Down syndrome chromosomal disorder 51 lymphocyte activation 51 somatization disorder 51 antiphospholipid antibodies 51 carcinoid 51 APOE gene 51 #q deletion 51 trisomy 51 hypermethylated 51 proteoglycan 51 ApoE4 51 dehydrogenase deficiency 51 PDGFRA 51 Wilm tumor 51 PFAPA 51 Arnold Chiari Malformation 51 brain malformation 51 exotropia 51 microencephaly 51 myoclonus 51 DIPG 51 Hemophilia B 51 Cushing syndrome 51 multisystemic 51 alpha thalassemia 51 Treg cell 51 aciduria 51 Myofascial pain 51 phenotypic variation 51 achromatopsia 51 invasive secretory carcinoma 51 autism spectrum disorders ASDs 51 Friedreich ataxia 51 Treponema 51 microRNAs miRNAs 51 beta1 integrin 51 homozygous FH 51 Gestational diabetes 51 malignant fibrous histiocytoma 51 variable immunodeficiency 51 hyperprolactinemia 51 neurological manifestations 51 skeletal malformations 51 neonatal encephalopathy 51 diabetes insipidus 51 LHON 51 TYMS 51 squamous cell lung cancer 51 compulsive hoarding 51 X chromosome inactivation 51 nasopharyngeal carcinoma 51 JMML 51 hypoplastic 51 Hurthle cell 51 facial clefts 51 DLX5 51 β thalassemia 51 chromosome 51 KLF4 51 Chronic pancreatitis 51 myeloproliferative diseases 51 placenta praevia 51 Glioblastomas 51 gestational diabetes mellitus 51 paroxysmal nocturnal hemoglobinuria 51 HER2 neu