Related by context. All words. (Click for frequent words.) 68 chromosomal defect 68 chromosome abnormality 67 chromosomal disorder 67 genetic abnormality 63 holoprosencephaly 62 neural tube defect 62 genetic abnormalities 62 trisomy 62 Joubert syndrome 62 anencephaly 61 IUGR 61 aneuploidies 61 rare chromosomal disorder 61 autosomal dominant 61 myelomeningocele 61 genetic mutation 61 Dravet syndrome 61 genetic defect 61 hydrops 61 gene mutation 61 congenital abnormality 60 pyloric stenosis 60 congenital anomaly 60 autosomal recessive 60 bronchopulmonary dysplasia 60 genetic disorder 60 Spina bifida 60 chromosomal disorders 59 congenital disorder 59 chromosomal anomaly 59 recessive gene 59 neurodevelopmental disorder 59 congenital abnormalities 59 spontaneous mutation 59 mosaicism 59 abnormalities 59 Angelman syndrome 59 MCAD deficiency 59 Hashimoto thyroiditis 59 developmental abnormalities 59 chromosomal abnormalities 59 achondroplasia 58 idiopathic 58 mutated gene 58 ectopic 58 abnormality 58 Beckwith Wiedemann syndrome 58 hypoplasia 58 ADPKD 58 Hirschsprung disease 58 congenital anomalies 58 inherited mutations 58 brain lesions 58 Tay Sachs disease 58 persistent pulmonary hypertension 58 DiGeorge Syndrome 58 intraventricular hemorrhage 58 cryptorchidism 57 mtDNA mutations 57 biliary atresia 57 hyperemesis gravidarum 57 IgA deficiency 57 Holoprosencephaly 57 amniotic fluid embolism 57 Apert syndrome 57 paraganglioma 57 congenital diaphragmatic hernia 57 Klinefelter syndrome 57 beta thalassemia 57 mutation 57 immunodeficiency 57 osteogenesis imperfecta 57 Wilms tumor 57 monozygotic twins 57 fetal malformations 57 Cockayne syndrome 57 autistic traits 57 hereditary disorder 57 congenital adrenal hyperplasia 57 congenital deafness 57 preterm deliveries 57 autosomal dominant disorder 57 microcephaly 57 defective gene 57 #q#.# deletion syndrome 57 de novo mutations 57 diaphragmatic hernia 57 DiGeorge syndrome 57 prenatally diagnosed 57 chromosome abnormalities 57 chromosomal alterations 56 neurodegenerative disorder 56 aneuploidy 56 brain malformation 56 choriocarcinoma 56 Congenital Adrenal Hyperplasia 56 NF1 56 Fanconi anemia 56 chorioamnionitis 56 Hurler syndrome 56 lymphangioleiomyomatosis LAM 56 inherited neurological disorder 56 Hurler Syndrome 56 autosomal recessive disease 56 malformation 56 congenital adrenal hyperplasia CAH 56 gastroschisis 56 hyperemesis 56 Noonan Syndrome 56 congenital disorders 56 CHD7 56 recurrent miscarriage 56 leukoencephalopathy 56 MECP2 gene 56 dysmorphic features 56 habitual snoring 56 congenital hypothyroidism 56 Li Fraumeni syndrome 56 hemolytic disease 56 Spinal muscular atrophy 56 septo optic dysplasia 56 recurrent miscarriages 55 endocrine disorder 55 genetic syndromes 55 MCADD 55 missense mutation 55 microdeletion 55 Cushing syndrome 55 thyroiditis 55 toxoplasmosis 55 skeletal dysplasia 55 pseudotumor cerebri 55 dilated cardiomyopathy 55 polycystic ovaries 55 malformations 55 proband 55 Ph chromosome 55 LQTS 55 mutant allele 55 atresia 55 sporadic ALS 55 ectodermal dysplasia 55 leiomyomas 55 autistic regression 55 mutant gene 55 HMGA2 55 recessive genes 55 chromosomal aberrations 55 pulmonary hypoplasia 55 PANDAS 55 paraneoplastic 55 fatal neurodegenerative 55 Trisomy 55 ambiguous genitalia 55 G#S mutation 55 heterozygous 55 oligohydramnios 55 transfusion syndrome 55 familial ALS 55 teratoma 55 chromosomal defects 55 hereditary deafness 55 Mycoplasma pneumoniae 55 degenerative disorder 55 polycystic ovary syndrome 55 Gestational diabetes 55 deletion 5q 55 BRCA2 gene 55 postnatally 55 karyotype 55 neurodevelopmental impairment 55 myositis 55 chromosomal anomalies 55 dysgenesis 55 PTPN# 55 Intussusception 55 fetal anomalies 55 Prader Willi syndrome 55 neurodevelopment disorder 55 febrile seizure 55 spontaneous mutations 54 germline mutations 54 epididymitis 54 VUR 54 FMR1 54 Anencephaly 54 polyhydramnios 54 Rh positive 54 sCJD 54 spinocerebellar ataxia 54 de ath 54 placental abruption 54 hypertrophic cardiomyopathy HCM 54 lactase deficiency 54 PNET 54 neuropsychiatric disorder 54 HbF 54 gene mutations 54 MELAS 54 neuroblastomas 54 subclinical hypothyroidism 54 synovial sarcoma 54 diagnosed prenatally 54 myotonic dystrophy 54 congenital malformations 54 fibrous dysplasia 54 histiocytosis 54 aplasia 54 polydactylism 54 placental malaria 54 monogenic 54 sporadic Creutzfeldt Jakob 54 heterotaxy 54 huntingtin gene 54 hypogonadotropic hypogonadism 54 chromosome deletion 54 mitochondrial dysfunction 54 Down syndrome chromosomal disorder 54 heart syndrome HLHS 54 homozygosity 54 combined immunodeficiency SCID 54 RhD negative 54 ependymoma 54 Pulmonary hypertension 54 genetic defects 54 molar pregnancy 54 AAT deficiency 54 Sanfilippo Syndrome 54 medulloblastoma 54 microdeletions 54 thrombophilia 54 JAK mutations 54 Joubert Syndrome 54 chorionic villus sampling 54 dyskeratosis congenita 54 enzyme deficiency 54 birth defect 54 tuberous sclerosis complex 54 Severe Combined Immunodeficiency 54 spastic diplegia 54 predisposing factor 54 hamartomas 54 Aplastic anemia 54 causative gene 54 CFTR gene 54 TEL AML1 54 NF2 54 JMML 54 polydactyly 54 primitive neuroectodermal tumors 53 APOE gene 53 Brugada syndrome 53 apolipoprotein E gene 53 blastoma 53 underactive thyroid gland 53 precocious puberty 53 neonate 53 singleton pregnancy 53 primary ciliary dyskinesia 53 carcinoid tumor 53 metabolic disorder 53 mitochondrial disorder 53 Obstructive sleep apnea 53 HNPCC 53 gene MECP2 53 somatic mutation 53 homozygotes 53 Beckwith Wiedemann Syndrome 53 mitochondrial disease 53 penetrance 53 Polycystic ovary syndrome 53 tricuspid atresia 53 extreme prematurity 53 polycystic kidneys 53 Cholangiocarcinoma 53 genetic mutations 53 allelic variants 53 cardiomegaly 53 germline mutation 53 clotting disorder 53 ovarian tumors 53 placental insufficiency 53 APOE4 53 #q#.# [001] 53 enterocolitis 53 breast carcinomas 53 recessive genetic 53 Niemann Pick disease 53 phthalate syndrome 53 precancerous condition 53 herpesviruses 53 atopy 53 fronto temporal dementia 53 uterus didelphys 53 monozygotic 53 Arrhythmogenic Right Ventricular Cardiomyopathy 53 Wiskott Aldrich syndrome 53 overt hypothyroidism 53 craniosynostosis 53 adnexal mass 53 ARVD 53 prion disease 53 Myocardial infarction 53 X chromosome 53 dizygotic twins 53 MeCP2 gene 53 galactosemia 53 genetically inherited 53 arrhythmogenic right 53 hyperplastic 53 karyotypes 53 neoplasm 53 neurofibromas 53 enteroviral infection 53 leukemia ALL 53 lissencephaly 53 #q deletion 53 heterozygotes 53 V Leiden 53 long QT syndrome 53 neuroblastoma 53 granule cells 53 intrauterine infection 53 idiopathic epilepsy 52 spontaneous remission 52 adrenal insufficiency 52 roseola 52 necrotizing enterocolitis 52 dizygotic 52 Lafora disease 52 Myopathy 52 genetic variant 52 atypical scrapie 52 Retinoblastoma 52 primary pulmonary hypertension 52 subclinical 52 somatic mutations 52 pulmonary atresia 52 Osteosarcoma 52 hormonal disorder 52 Moyamoya disease 52 optic nerve hypoplasia 52 juvenile myelomonocytic leukemia 52 lymphocytic 52 CMV infection 52 blood clotting disorder 52 Eisenmenger syndrome 52 supratentorial 52 recessive inheritance 52 HGPS 52 TP# mutations 52 polycystic ovary syndrome PCOS 52 neonatal encephalopathy 52 homozygous 52 Newborn screening 52 adrenal cortex 52 sirenomelia 52 BRCA2 mutation 52 fatal neurodegenerative disorder 52 chronic granulomatous disease 52 hemophagocytic lymphohistiocytosis 52 congenital scoliosis 52 autosomal recessive disorder 52 esophageal atresia 52 congenital hydrocephalus 52 Fragile X Syndrome 52 myopathy 52 rs# [002] 52 #q 52 Biliary atresia 52 Cerebral palsy 52 periventricular leukomalacia 52 BRCA1 mutations 52 PrPSc 52 Klinefelter Syndrome 52 monozygotic twin 52 polymorphic ventricular tachycardia 52 CDH1 52 acute lymphoid leukemia 52 preeclamptic 52 testicular tumors 52 Bardet Biedl syndrome 52 hereditary predisposition 52 Myocarditis 52 facial clefts 52 APOE e4 52 malignant neoplasm 52 aY chromosome 52 alveolar rhabdomyosarcoma 52 Kufs disease 52 medulloblastomas 52 uterine tumors 52 familial adenomatous polyposis 52 chromosomal instability 52 SRY gene 52 hyperbilirubinemia 52 HLA B# 52 genetic neuromuscular disorder 52 untreated celiac disease 52 CNVs 52 immunodeficiency disorder 52 FMR1 gene 52 Pre eclampsia 52 Neuregulin 1 52 Pervasive Developmental Disorder 52 malignant lymphoma 52 PPHN 52 situs inversus 52 WAGR syndrome 52 antenatal depression 52 dentate gyrus 52 myeloproliferative neoplasms 52 mutations 52 Myotonic dystrophy 52 TTTS 52 Polycystic ovary syndrome PCOS 52 Hypoplastic Left Heart 52 Hyperthyroidism 52 abnormal chromosomes 52 fetu 52 Wilm tumor 52 hypothyroid 52 #q# [001] 52 LVNC 52 PTLD 52 Fanconi Anemia 52 chromosome 52 graft dysfunction 52 twin transfusion 52 Hutchinson Gilford progeria 52 Wolf Hirschhorn 52 inherited genetic mutation 52 IPAH 52 Coeliac disease 52 orchitis 52 Dysplasia 52 KCNE2 52 dwarfism 52 chromosomal translocations 52 neurodevelopmental 52 Heavy menstrual bleeding 52 behavioral disinhibition 52 CHDs 52 peripartum cardiomyopathy 52 thyroid hormone deficiency 52 myometrium 52 Eclampsia 52 Crouzon Syndrome 52 Sandhoff disease 51 autosomal dominant inheritance 51 Brugada Syndrome 51 neurological abnormalities 51 LV dysfunction 51 phenotype 51 Chiari Malformation 51 fertilized egg splits 51 intestinal biopsy 51 xeroderma pigmentosum 51 lysosomal storage disease 51 X inactivation 51 progressive neurodegenerative disorder 51 MLL gene 51 hamartoma 51 Rb gene 51 agenesis 51 Diamond Blackfan anemia 51 heritable 51 ABCB1 51 alleles 51 ASDs 51 ovarian hyperstimulation syndrome OHSS 51 BRCA1 gene 51 lymphoblastic leukemia 51 recessive trait 51 Rett syndrome 51 5q deletion 51 unexplained infertility 51 Amniocentesis 51 BRCA1 mutation 51 preterm delivery 51 Sporadic CJD 51 truncus arteriosus 51 pheochromocytoma 51 Cowden syndrome 51 GH deficiency 51 periventricular 51 neural tube 51 neurologic complications 51 neuro developmental disorder 51 dysmotility 51 Chiari malformation 51 airway hyperresponsiveness 51 acute leukemias 51 chromosomal rearrangement 51 irregular menstrual periods 51 severe aplastic anemia 51 bacteraemia 51 Male pattern baldness 51 blastomeres 51 chromosome #q#.# [001] 51 involuntary tics 51 childhood disintegrative disorder 51 Vitamin B# deficiency 51 angiosarcoma 51 hypertrophic cardiomyopathy 51 preeclampsia 51 neurological manifestations 51 Rh incompatibility 51 FTLD 51 Uterine fibroids 51 Arnold Chiari Malformation 51 idiopathic pulmonary arterial hypertension 51 BARD1 51 neurobiological disorder 51 narcolepsy cataplexy 51 microvascular angina 51 BRCA mutation 51 aciduria 51 intra uterine 51 Multivariate analysis 51 ultra rapid metabolizer 51 eosinophilic esophagitis 51 atherosclerotic lesion 51 undiagnosed celiac disease 51 frontotemporal dementia 51 gene locus 51 superfetation 51 inherited predisposition 51 gastric distention 51 fetal abnormalities 51 Peutz Jeghers syndrome 51 systemic scleroderma 51 microsatellite instability 51 mammary tumors 51 pathogenic mutations 51 ataxia telangiectasia 51 severe congenital neutropenia 51 susceptibility gene 51 malignant transformation 51 intestinal inflammation 51 GISTs 51 von Willebrand disease 51 growth restriction IUGR 51 Mendelian disorders 51 nonsense mutations 51 neuroblastoma tumor 51 epigenetic alterations 51 LRRK2 mutations 51 undescended testicles 51 IKZF1 51 Dwarfism 51 toxemia 51 atypical hyperplasia 51 aneuploidy screening 51 Medulloblastoma 51 Meckel Gruber 51 brachial plexus palsy 51 fructose intolerance 51 RhD 51 tubal pregnancy 51 ectopic pregnancies 51 maternally inherited 51 umbilical artery 51 subarachnoid haemorrhage 51 leptin receptor 51 oral clefts 51 gastric carcinoma 51 congenital malformation 51 epigenetic changes 51 hypotonia 51 euthymic patients 51 astrocytomas 51 CagA 51 MYH9 gene 51 pre eclamptic 51 polymyalgia rheumatica 51 Rh negative 51 Morquio syndrome 51 familial hypercholesterolemia 51 TACI 51 clinically insignificant 51 idiopathic generalized epilepsy 51 hereditary hemochromatosis 51 biliary atresia rare 51 dominantly inherited 51 medulloblastoma tumors 51 serum IGF 51 nonsense mutation 51 acute myocarditis 51 G6PD deficiency 51 Loeys Dietz syndrome 51 Acute Myeloid Leukaemia 51 Polycystic Ovarian Syndrome PCOS 51 nephritis 51 SHANK3 51 seropositivity 51 perinatal mortality 51 mesotheliomas 51 pancytopenia 51 chromosomal imbalance 51 hyperinsulinemia 51 K ras mutations 51 Toxoplasmosis 51 rs# [004] 51 Genetic predisposition 51 spasmodic dysphonia 51 medium chain acyl 51 hypopituitarism 51 syndrome FAS 51 otosclerosis 51 GSTT1 51 extrapyramidal symptoms 51 atypia 51 born preterm 51 pre eclampsia 51 MLH1 51 Heterozygous 50 pheochromocytomas 50 phenylketonuria 50 dermoid cyst 50 NNRTI resistance 50 familial aggregation 50 herpes infection 50 congenital muscular dystrophy 50 Progeria 50 atherosclerotic lesions 50 neurofibroma 50 WNK1 50 ApoE4 gene 50 primary biliary cirrhosis 50 Langerhans cell histiocytosis 50 cytogenetic abnormalities 50 postpartum hemorrhage 50 chromosome rearrangements 50 MSH2 50 prosopagnosia 50 TACI mutations 50 Thrombocytopenia 50 receptor gene 50 Krabbe Disease 50 stillbirth 50 fusiform 50 Congenital 50 Leukemias 50 incompetent cervix 50 Spasmodic dysphonia 50 hyperparathyroidism 50 coinfection 50 parkin gene 50 Wegener granulomatosis 50 spinocerebellar ataxia type 50 mammary gland tumors 50 immunoreactivity 50 Alagille syndrome 50 microcephalin 50 etiologic 50 subclinical hyperthyroidism 50 tics involuntary 50 thyroid dysfunction 50 BRCA gene mutation 50 Irritable bowel syndrome 50 primary ovarian insufficiency 50 GBA mutations 50 cloacal exstrophy 50 spastic paraplegia 50 autistic tendencies 50 CHARGE syndrome 50 Hirschsprung Disease 50 prenatal ultrasound 50 RSV infections 50 dysplasia 50 adenocarcinomas 50 poorer prognosis 50 familial pancreatic cancer 50 neurologic disorder 50 DNA methylation patterns 50 thyroid hormone levels 50 embryonal rhabdomyosarcoma 50 Aortic dissection 50 dysplastic 50 autoantibodies 50 corpus luteum 50 Prox1 50 SOX3 gene 50 rhabdomyosarcoma 50 gene expression patterns 50 nerve degeneration 50 lymphatic tissue 50 pAkt 50 mitochondrial diseases 50 premature menopause 50 Polycystic kidney disease 50 bicuspid valve 50 follicle stimulating hormone 50 variable immunodeficiency 50 dyscalculia 50 myopathies 50 functional polymorphism 50 clefting 50 CNTNAP2 50 MYCN 50 IL#R 50 epigenetic modification 50 lichen planus 50 Proteus syndrome 50 IGF1 50 rhesus 50 FXTAS 50 infantile hemangiomas 50 congenital CMV 50 hypoplastic 50 hypoperfusion 50 Endometrial cancer 50 static encephalopathy 50 Polycystic Ovary Syndrome 50 gestational diabetes mellitus GDM 50 leiomyoma 50 diabetes mellitus T2DM 50 SMN1 50 preeclamptic women 50 ependymomas 50 generalized epilepsy 50 systemic mastocytosis 50 superinfection 50 autism spectrum disorder 50 Hurthle cell 50 essential thrombocythemia 50 utero 50 skeletal malformations 50 SLC#A# [002] 50 retinal dysfunction 50 pyelonephritis 50 profound deafness 50 BRCA mutations 50 UGT#A# * 50 cerebellar hypoplasia 50 chromosomal translocation 50 dysbindin 50 antiphospholipid antibodies 50 Bacterial vaginosis 50 highly heritable 50 thrombocytosis 50 hyperactivated 50 apolipoprotein E 50 hydrocephaly 50 SNHL 50 abnormal prions 50 Aortic stenosis 50 missense mutations 50 myocarditis 50 febrile convulsions 50 chronic eosinophilic leukemia 50 downregulation 50 gastric adenocarcinoma 50 activating mutations 50 degenerative nerve disorder 50 ZNF# 50 cervical lymph nodes 50 kisspeptin 50 granulosa cell 50 neonatal morbidity 50 perinatal asphyxia 50 idiopathic PAH 50 hepatoblastoma 50 cardiac hypertrophy 50 placenta previa 50 thyroglobulin 50 BMPR2 50 haplotype 50 Cystic fibrosis 50 chromosome #q# [002] 50 tryptophan depletion 50 #q# deletion 50 multisystem disorder 50 Tourette syndrome neurological disorder 50 Fas ligand 50 Aicardi syndrome 50 post natally 50 intractable epilepsy 50 Krabbe leukodystrophy 50 uterine rupture 50 polycystic ovarian syndrome 50 APOL1 50 homozygous FH 50 infectious mononucleosis 50 degenerative neurological disorder 50 diabetes insipidus 50 EoE 50 acute rheumatic fever 50 Hutchinson Gilford Progeria Syndrome 50 BRCA2 gene mutation 50 hypoxic ischemic encephalopathy 50 ApoE gene 50 HLA identical 50 recurrent UTI 50 asymptomatic 50 mice lacking 50 mRNA transcripts 50 overactivity 50 Ovarian cysts 50 alpha thalassemia 50 filaggrin 50 eosinophilic 50 ovarian dysfunction 50 Severe Primary IGFD 50 p# mutation 50 MGUS 50 Cervical dystonia 50 prepubertal 50 neurologic deficits 50 Epstein Barr virus EBV 50 Hypothyroidism 50 thyroid nodules 50 interferon pathway 50 hydronephrosis 50 frameshift mutation 49 enteroviral 49 deleterious mutation 49 Bronchiolitis 49 placenta praevia 49 PPCM 49 haplotypes 49 FSGS 49 JAK2 gene 49 mammary cells 49 mutant protein 49 mutated protein 49 anal incontinence 49 Angelman Syndrome 49 neuritic 49 leukoencephalopathy PML 49 recessive dystrophic epidermolysis bullosa 49 inherited neurodegenerative disorder 49 genital abnormalities 49 heavy menstrual bleeding 49 gene variants 49 Kabuki syndrome 49 CNTNAP2 gene 49 FASPS 49 Foetal Alcohol Spectrum Disorder 49 endostatin 49 urethritis 49 microbleeds 49 adenoma 49 polycystic disease 49 beta globin 49 mental retardation epilepsy 49 Foxp3 49 infarcts 49 Sjögren syndrome 49 Henoch purpura 49 prenatally 49 abruption 49 Iron deficiency anemia 49 CC genotype 49 post partum psychosis 49 arterial calcification 49 auditory neuropathy 49 recurrent wheezing 49 stem glioma 49 dysautonomia 49 systemic amyloidosis 49 rheumatic disease 49 dystrophy 49 incurable neurological disorder 49 primitive neuroectodermal tumor 49 monoclonal gammopathy 49 Rh factor 49 genetic heterogeneity 49 nonischemic 49 Postnatal depression 49 causative genes 49 enterovirus infection 49 rs# [003] 49 prolonged QT interval 49 lacunar 49 limb deformities 49 cerebral infarction 49 undergoing hysterectomy 49 Idiopathic 49 mitochondrial mutations 49 paragangliomas 49 Preeclampsia 49 folate deficiency 49 fetal chromosomal 49 acetabular dysplasia 49 cystic lesions 49 meconium 49 Genetic variants 49 hemangioma 49 abnormal chromosome 49 Krabbe disease 49 endometritis 49 neoplasias 49 fetal echocardiogram 49 congenital brain tumor 49 velo cardio facial 49 Fragile X syndrome 49 subfertility 49 POMC neurons 49 chiari malformation 49 allele frequency 49 EBV infection 49 hirsutism 49 varicoceles 49 SRBD 49 Abnormalities 49 sonographically 49 perioperative complications 49 mesenteric 49 myeloproliferative 49 proto oncogene 49 non syndromic 49 nonhereditary 49 measles virus 49 CREBBP 49 unexplained mental retardation 49 hyperprolactinemia 49 STAT4 49 malignant glioma brain tumor 49 ectopia cordis 49 muscle degeneration 49 Hydrocephalus 49 cranial irradiation 49 BRCA1 mutation carriers 49 Genital herpes 49 birthweight 49 pituitary tumors 49 tuberous sclerosis 49 Cryptococcus neoformans 49 aortic insufficiency 49 Hemochromatosis 49 hepatitis B infection 49 lactose malabsorption 49 Beta thalassemia 49 paresis 49 adrenal function 49 p# mutations 49 myelogenous leukemia 49 microchimerism 49 teratogens 49 Mental retardation 49 PDGFRA 49 Mitochondrial diseases 49 recessive mutations 49 azoospermia 49 APOE ε4 49 Leber congenital amaurosis 49 nulliparous 49 #p# [001] 49 embryonal 49 Neurofibromatosis type 49 CYP#E# gene 49 hypermethylated 49 Folate deficiency 49 amenorrhea 49 cryptogenic 49 neurologic symptoms 49 HFE gene 49 immunodeficiencies 49 mutant alleles 49 spontaneous abortions 49 aortic regurgitation 49 hyperactivation 49 Idiopathic Thrombocytopenic Purpura ITP 49 autoimmune hemolytic anemia 49 amenorrhoea 49 deformational plagiocephaly 49 G6PD 49 Hip dysplasia 49 antral follicles 49 parkinsonism 49 human metapneumovirus 49 germline cells 49 genetic trait 49 TP# gene 49 Hereditary angioedema HAE 49 lysosomal diseases 49 G allele 49 developmental disorder 49 severe hyperbilirubinemia 49 gene rearrangements 49 motor neuron degeneration 49 prognostic factor 49 lobular breast cancer 49 SOD1 gene 49 embryo biopsy 49 HLHS 49 % CI #.#-#.# [007] 49 hypomethylation 49 utero exposure 49 Retinopathy 49 rs# [001] 49 SLC#A# gene [001] 49 underlying pathophysiology 49 Hypertrophic cardiomyopathy 49 Reye syndrome 49 anatomical abnormalities 49 paralytic illness