Related by context. All words. (Click for frequent words.) 65 breast cancer genes BRCA1 64 cause cardiac channelopathies 64 BRIP1 64 inherited mutations 64 BRCA1 BRCA2 63 Apolipoprotein E4 62 BRCA2 mutations 62 mutated BRCA1 62 Folate deficiency 62 mutated BRCA 62 BRCA2 mutation 62 BRCA1 gene 62 BRCA2 gene 62 apolipoprotein E4 61 BRCA2 gene mutation 61 CCR5 delta# 61 C#Y 61 MTHFR 61 MYH9 gene 60 BRCA1 60 apolipoprotein E gene 60 BARD1 60 genes BRCA1 60 apolipoprotein E 60 BRCA1 mutations 60 BRCA gene mutation 59 abnormal methylation 59 IgA deficiency 59 CDKN2A 59 Fragile X gene 59 SHANK3 59 Heterozygous 59 APOE epsilon 4 59 irregular menstrual cycles 59 Ribavirin causes 58 APOE e4 58 BMPR2 58 Li Fraumeni 58 V Leiden 58 Tay Sachs thalassemia 58 BRCA2 gene mutations 58 chronic granulomatous disease 58 testicular germ cell 58 untreated hypothyroidism 58 ApoE4 gene 58 CDH1 58 dysplastic lesions caused 58 Kufs disease 58 c KIT 58 CYP#C# * 58 UGT#A# * 58 KIF6 gene 58 MSH2 58 breast endometrial 58 K ras mutations 58 hepatic lipase 58 Carcinoid tumors 57 testicular tumors 57 5 HT2A serotonin 57 chromosomal disorders 57 TP# gene 57 progranulin gene 57 Colon polyps 57 microdeletion 57 KRAS oncogene 57 without uremia 57 sickle cell cystic fibrosis 57 interferon pathway 57 chromosomal rearrangement 57 hereditary predisposition 57 premature ovarian 57 APOE4 57 cystic fibrosis sickle cell 57 lymphomas leukemias 57 PTPN# 57 IL#R 57 MLH1 57 Li Fraumeni syndrome 57 transfusion syndrome 56 tryptase 56 regulator CFTR gene 56 autosomal recessive 56 anaplastic lymphoma kinase 56 apolipoprotein E APOE 56 GSTT1 56 Genetic mutations 56 APOE allele 56 BRCA mutation 56 MLL2 56 CHEK2 56 induced mucositis 56 hereditary hemochromatosis 56 familial hypercholesterolemia 56 abnormal lipid levels 56 CYP#A# CYP#D# 56 COX2 56 Hashimoto thyroiditis 56 ABCB1 56 BRCA genes 56 III EGFRvIII 56 gene BRCA2 56 7F 9V 56 Strong inducers 56 HFE gene 56 autosomal recessive disease 56 Polycystic ovary syndrome PCOS 56 prostate pancreatic 56 Genetic variations 56 myeloproliferative neoplasms 56 * 1F 56 BRCA2 56 gestational diabetes mellitus 56 multiple sclerosis psoriasis 56 TCF#L# gene 56 muscular dystrophy cystic fibrosis 56 Cystic fibrosis CF 56 p# mutation 56 pancreas esophagus 56 familial adenomatous polyposis 56 dominantly inherited 56 Systemic lupus erythematosus 56 certain protein tyrosine 56 apoC III 55 severe congenital neutropenia 55 pancreatic prostate 55 FGFR2 55 germline mutations 55 Apolipoprotein E 55 lupus scleroderma 55 LRAT 55 HLA DRB1 55 GRK5 55 G#S mutation 55 HNPCC 55 impair fertility 55 premature menopause 55 TGFBR1 * 6A 55 hypokalemia hypomagnesemia 55 genital human papillomavirus 55 deafness neurological 55 autosomal recessive disorder 55 primary ovarian insufficiency 55 HLA DQ2 55 pancreatic endocrine 55 mutated K ras 55 gastrointestinal stromal 55 IGF binding 55 BRCA1 mutation 55 dopamine D4 receptor 55 Maternal obesity 55 subependymal giant cell 55 ε4 55 Colorectal cancers 55 cholesteryl ester transfer 55 normal karyotype 55 underactive thyroid gland 55 untreated celiac disease 55 autosomal dominant disorder 55 TSC1 55 genus Plasmodium 55 included exfoliative dermatitis 55 ApoE4 allele 55 MECP2 gene 55 endometriosis ovarian cysts 55 autoimmune thyroid 55 BRAF V#E 55 G6PD deficiency 55 gene predisposing 55 CYP# [002] 55 genes predisposing 55 chromosomal defects 55 genotoxic stress 55 TACI mutations 55 Pulmonary hypertension 55 CFTR gene 55 polycystic ovarian disease 55 dopamine receptor gene 55 noncarriers 55 #q# deletion 55 fetal malformations 55 decompensated liver disease 55 ovarian dysfunction 55 K ras gene 55 HLA DRB1 SE 55 APOL1 54 CYP#D# gene 54 aneuploidy 54 chorioamnionitis 54 SCN5A 54 rheumatoid arthritis inflammatory bowel 54 ENPP1 54 Pelvic inflammatory 54 de novo mutations 54 AML MDS 54 missense mutation 54 Pten 54 hormonally sensitive 54 Asymptomatic 54 phthalate syndrome 54 leukaemias 54 Selenium deficiency 54 Premature Aging 54 UGT#B# 54 RUNX3 54 persistent pulmonary hypertension 54 Von Willebrand disease 54 HPV vaccine protects 54 BCL#A 54 hypermethylated 54 nonhereditary 54 familial pancreatic cancer 54 used DNA alkylating 54 Clusterin 54 Am J Clin 54 Genetic predisposition 54 Selective serotonin reuptake inhibitors 54 mental retardation epilepsy 54 fat malabsorption 54 nucleus Chinnery 54 tumor suppressors cytokines 54 Celiac sprue 54 mosaicism 54 TNF blocker therapy 54 MC4R gene 54 homocystinuria 54 leptin deficiency 54 atypical hyperplasia 54 JAK2 enzyme 54 resistin 54 susceptibility gene 54 microcephalin 54 Spinal muscular atrophy 54 chromosomal aberration 54 ADH1B 54 Low density lipoprotein 54 GPC5 54 spinal muscle atrophy 54 transferrin saturation 54 progesterone receptor negative 54 MLL gene 54 LRP5 54 reproductive abnormalities 54 plasminogen activator inhibitor 54 LRRK2 gene 54 gastric carcinogenesis 54 Lesch Nyhan syndrome 54 COPEGUS therapy 54 ApoE4 54 gene mutations 54 inherited predisposition 54 recessive genetic disorders 54 elevated triglyceride levels 54 carbohydrate intolerance 54 Joubert syndromes 54 5 6A 6B 54 Soy isoflavones 54 homozygous 54 carry BRCA mutation 54 Vitamin D insufficiency 53 CHD7 53 APOE gene 53 aldehyde dehydrogenase 53 monozygotic twin 53 mutated gene 53 Vitamin B# deficiency 53 BRAF gene mutations 53 recessive mutations 53 nonsense mutation 53 genetic abnormalities 53 Gestational 53 BRAF gene 53 gene rearrangements 53 intestinal polyps 53 epigenetic changes 53 homozygotes 53 heritable genetic 53 5 HTTLPR 53 prolonged QT interval 53 endocrine abnormalities 53 Suicidal tendencies 53 Treg cell 53 onset idiopathic hypogonadism 53 CYP #A# 53 cyclin dependent kinase inhibitor 53 known teratogen substance 53 infertility miscarriage 53 Erythropoietic therapies may 53 Polycystic Ovarian Syndrome PCOS 53 polyp recurrence 53 methylenetetrahydrofolate reductase 53 atopic disease 53 aneuploidies 53 KIBRA 53 Leukemias 53 overactivated 53 huntingtin gene 53 trophoblastic 53 DQB1 * 53 PLX STROKE targeting 53 paraoxonase 53 chromosomal anomalies 53 Raf MEK ERK 53 Autoimmune disorders 53 Cryptococcus neoformans 53 APOE ε4 53 gestational hypertension 53 familial hypercholesterolemia FH 53 deafness meningitis 53 ADH1B * 53 thalassemia sickle cell 53 Janus kinase 53 neural tube defect 53 non polyposis colorectal 53 homozygous FH 53 GABRA2 53 6 phosphate dehydrogenase 53 p# mutations 53 macrophage migration inhibitory 53 thyroid deficiency 53 Peutz Jeghers syndrome 53 TP# mutation 53 Malignant mesothelioma 53 maternally inherited 53 genital abnormalities 53 #q#.# [001] 53 Myostatin 53 DAT1 53 klotho 53 Basal Cell 53 dyskeratosis congenita 53 Levels Linked 53 receiving immunosuppressive therapy 53 rheumatoid arthritis lupus 53 polycystic ovarian syndrome PCOS 53 syngeneic 53 monocyte chemoattractant protein 53 chromosomal aberrations 53 severe dehydrating diarrhea 53 ABCB1 gene 53 autoimmune thyroiditis 53 OPRM1 gene 53 TTR gene 53 allelic variants 53 Tay Sachs disease 53 autoimmune disorder characterized 53 ApoE gene 53 Kluger Lexus GS# Lexus 53 hypothalamic amenorrhea 53 postoperative delirium 53 Meckel Gruber 53 Rh incompatibility 53 SMN1 53 heterozygotes 53 GNAQ 53 VHL gene 53 shorter telomere length 53 bacteria Neisseria meningitidis 53 Bronchopulmonary Dysplasia 53 HGPS 53 Phytoestrogens 53 developmental abnormalities 53 TCF#L# 53 gastric carcinoma 53 deCODE BreastCancer 53 Mg Usa 53 NPC1 53 shortened telomeres 53 PALB2 53 PDGFR 53 NKX2 53 familial dysautonomia 53 myopathies 52 C1 INH deficiency 52 cystic fibrosis muscular dystrophy 52 impaired glucose metabolism 52 Genetic variation 52 CYP#C# [002] 52 BRCA mutations 52 systemic juvenile idiopathic 52 parkin gene 52 TNFAIP3 52 5 HT1A receptor 52 autoinflammatory diseases 52 BRCA 52 hormone refractory prostate 52 Cyclooxygenase 2 52 Mg Uk 52 granulosa cell 52 post transplant lymphoproliferative 52 HLA DRB1 * 52 genetic polymorphism 52 CYT# potent vascular disrupting 52 Tuberous sclerosis 52 Endometrial cancer 52 penetrance 52 placental function 52 Zinc deficiency 52 V#F mutation 52 thrombophilia 52 ZNF# 52 mtDNA mutations 52 Systemic lupus erythematosus SLE 52 APOC3 52 dyslipidemia abnormal 52 severe malignant osteopetrosis 52 recessive genetic 52 Iron deficiency 52 Prolactin 52 bacterium Neisseria meningitidis 52 SOD2 gene 52 Chronic pancreatitis 52 Polymorphic Ventricular Tachycardia CPVT 52 multifactorial disease 52 gene mutation 52 medulloblastoma tumors 52 cirrhosis liver failure 52 recurrent UTI 52 MEF2A 52 insulin resistance syndrome 52 thyrotropin 52 lipoprotein metabolism 52 Bacterial vaginosis 52 Human papilloma virus 52 anaphylactic reactions bronchospasm 52 gallstone disease 52 monogenic 52 TMEM#B 52 STAT4 52 MC1R 52 cystic fibrosis Duchenne muscular 52 Acute pancreatitis 52 Acute Exacerbations 52 Chronic ITP 52 proband 52 angioneurotic edema 52 shorter telomeres 52 nonsense mutations 52 Breastfed infants 52 Human papillomavirus HPV 52 GSTM1 52 overt hepatic encephalopathy HE 52 lymphocyte activation 52 polycystic ovary syndrome 52 lactalbumin 52 gene variant 52 GAB2 52 endogenous hormones 52 hereditary nonpolyposis colon cancer 52 hyperparathyroidism 52 bexarotene 52 Muscular dystrophies 52 lethargy irritability 52 Fibroblast growth 52 recurrent wheezing 52 slow metabolizers 52 hydrops 52 nonhematologic adverse reactions 52 hormone receptor negative 52 Acute myeloid leukemia 52 kidney urologic 52 PTP1B 52 osteosarcomas 52 Cognitive impairment 52 inherit predisposition 52 collagen vascular 52 diarrhea abdominal cramps nausea 52 overactive thyroid gland 52 J Antimicrob Chemother 52 congenital deficiency 52 oral clefts 52 deletion 5q 52 genetic syndromes 52 PTEN gene 52 mutant allele 52 predisposing 52 inherited neurodegenerative 52 congenital disorders 52 rheumatoid arthritis systemic lupus 52 chromosomal abnormalities 52 hyperinsulinemia 52 Glucocorticoids 52 Genetic variants 52 clefting 52 ambiguous genitalia 52 N Engl J 52 mutation 52 Ets2 52 Autoantibodies 52 rs# [004] 52 melanocortin receptor 52 Predisposition 52 bacteria Helicobacter pylori 52 Yeast infections 52 breast tenderness bloating 52 Study Spacing 52 SMN1 gene 52 SORL1 52 HMG CoA reductase inhibitors 52 ORMDL3 52 precancerous cervical 52 progressive neurodegenerative disorder 52 1 diabetes T1D 52 Apert syndrome 52 elevated fasting glucose 52 cystic ovaries 52 Arch Intern Med 52 JAK2 gene 52 CXCL5 52 cystic fibrosis chronic pancreatitis 52 LIS1 52 Interferon gamma 52 human papilloma viruses 52 hormonal abnormalities 52 CETP VV 52 SOD1 gene 52 selective modulator 52 serum aminotransferase levels 52 Polymorphisms 51 genetic defects 51 cytomegalovirus CMV 51 BRCA gene 51 CYP#A# [002] 51 neuroblastoma tumors 51 leukemia multiple myeloma 51 J Am Acad 51 non syndromic 51 Chlamydia psittaci 51 Gastroesophageal reflux disease 51 human papillomaviruses HPV 51 lupus rheumatoid arthritis 51 LDLR 51 chronic rheumatic 51 leiomyomas 51 Fas ligand 51 parasite Trypanosoma cruzi 51 hormones progesterone 51 #:#-# [023] 51 ALK gene 51 GRNOPC1 contains 51 elevated triglycerides 51 intraventricular hemorrhage 51 Nonalcoholic fatty liver 51 KCNH2 51 gene polymorphism 51 content VENDOR WHITE PAPER 51 cystic fibrosis transmembrane conductance 51 PON1 51 chromosomal anomaly 51 male hormone androgen 51 lowers homocysteine 51 glaucoma ischemia 51 Ashkenazi Jewish 51 fronto temporal dementia 51 Neural tube defects 51 d l leucovorin 51 maternally transmitted 51 HIV HCV coinfected 51 Hereditary angioedema HAE 51 Androgenetic alopecia 51 MELAS 51 chromosomal instability 51 chromosomal defect 51 apo E 51 recessive trait 51 Lafora disease 51 Chlamydia pneumoniae 51 heartburn regurgitation 51 LMNA 51 catechol O methyltransferase COMT 51 #q#.# deletion syndrome 51 inflammatory PDE 51 infertility ectopic pregnancy 51 CYP#A# substrate 51 GSTP1 51 CRM# Protein 51 myelodysplastic myeloproliferative diseases 51 pharmacological chaperone compounds 51 Subclinical 51 familial predisposition 51 alpha1 51 cardiac hypertrophy 51 TNF Blockers 51 Nonsteroidal anti inflammatory 51 inhibit CYP#A# 51 congenital toxoplasmosis 51 Secondhand smoke exposure 51 MTHFR gene 51 #A #F 51 Von Willebrand 51 cyclin E 51 Moraxella catarrhalis 51 Acute lymphoblastic leukemia 51 type 1diabetes 51 Hutchinson Gilford progeria 51 Streptococcus pneumoniae Haemophilus influenzae 51 mitochondrial mutations 51 progerin 51 undescended testicles 51 polycystic ovary syndrome PCOS 51 TRAF1 C5 51 microdeletions 51 Arch Pediatr Adolesc Med 51 Oxidative stress 51 NF1 51 REGIONAL THEATER TONY AWARD 51 coinfection 51 polyhydramnios 51 Arrhythmogenic Right Ventricular Cardiomyopathy 51 autoinflammatory 51 T1DM 51 Von Hippel Lindau 51 LPA gene 51 associated tremor ataxia 51 heterotaxy 51 Penile cancer 51 lipid elevations 51 folate metabolism 51 nonischemic 51 Beta thalassemia 51 AMACR 51 receiving chemoradiation therapy 51 APOA5 51 takes ethosuximide 51 BRAF protein 51 renovascular hypertension 51 Eur J Endocrinol 51 IDH mutations 51 Hyperthyroidism 51 maternally derived 51 tumor suppressor protein 51 aneuploid 51 hereditary deafness 51 e4 allele 51 NOTCH1 51 CALHM1 51 Peptide YY 51 hereditary nonpolyposis colorectal cancer 51 asymptomatic bacteriuria 51 overexpress 51 chitinase 51 AAT Deficiency 51 Neurofibromatosis type 51 urethritis 51 Invasive pneumococcal disease 51 EGFR gene 51 diseases chronic granulomatous 51 abdominal adiposity 51 sexually transmitted HPV 51 J Am Coll 51 neonatal lupus 51 immuno suppressed 51 Long acting beta2 51 SGPT 51 Heredity 51 germline mutation 51 radiosensitive 51 CHRNA5 gene 51 seizures comas 51 meningitis encephalitis 51 APOE e4 gene 51 Emtriva Viread 51 narcolepsy cataplexy 51 oligodendrogliomas 51 chromosome abnormality 51 mutant huntingtin protein 51 filaggrin gene 51 heterozygous 51 CYP#A# isoenzyme 51 Selective Inhibitor 51 Gene Mutation 50 oesophageal adenocarcinoma 50 Oxidative damage 50 IUGR 50 immunocompetent adults 50 secondary amenorrhea 50 Aplastic anemia 50 pancreas pancreatitis 50 severe hepatic dysfunction 50 thromboxane A2 50 treatment emergent hyperglycemia 50 Reye syndrome rare 50 # HS webwire 50 abnormal clotting 50 Vidaza ® 50 neurodevelopment disorder 50 Avandia Actos 50 ALDH2 50 induce orthostatic hypotension 50 neuroligins 50 EMRISE Annual Report 50 phenylketonuria 50 ADPKD 50 familial polyposis 50 ovarian hyperstimulation syndrome OHSS 50 Antisocial personality 50 Fatty liver 50 Viral infections 50 Hepatitis B Virus 50 dysregulated 50 obstructive coronary 50 Smad7 50 unexplained vaginal bleeding 50 coinfected 50 rs# [002] 50 spinocerebellar ataxia 50 metabolic disturbances 50 PDE# 50 Smoking Linked 50 CC genotype 50 Congenital Adrenal Hyperplasia 50 polycystic ovaries 50 Igf2 50 missense mutations 50 Aortic stenosis 50 inhibiting COX 50 Epidermal Growth Factor Receptor 50 CYP#D# genotype 50 anal cancers 50 disease NAFLD 50 inducible nitric oxide synthase 50 familial ALS 50 MYCN amplification 50 anemias 50 varicella chickenpox 50 #q# [001] 50 upregulate 50 reduce serum phosphate 50 gene MECP2 50 Magnesium deficiency 50 Listeria infections 50 BRCA1 gene mutation 50 Fanconi anemia FA 50 Darapladib 50 Hypertrophic cardiomyopathy 50 serum IGF 50 INF2 50 Met receptor tyrosine 50 endogenous estrogen 50 HMGA2 50 myostatin gene 50 galactosemia 50 Progenitor cells 50 rs# [001] 50 orthostatic hypotension cataracts 50 Joubert syndrome 50 histologic subtype 50 genomic variants 50 MeCP2 gene 50 AAT deficiency 50 genetic abnormality 50 lung adenocarcinoma 50 neuro developmental disorders 50 C EBP alpha 50 Childhood Disorder 50 genetic variant 50 acute lymphoid leukemia 50 asymptomatic carriers 50 hypovitaminosis D 50 Genetic mutation 50 pyridoxine 50 Calcium intake 50 Am J Obstet 50 pneumococci 50 Ras oncogene 50 coma convulsions 50 causative gene 50 NF1 gene 50 CETP gene 50 Cockayne syndrome 50 epididymitis 50 pRb 50 Commonly prescribed 50 Human metapneumovirus 50 mutations 50 SRY gene 50 Loeys Dietz syndrome 50 precocious puberty 50 pleiotropic 50 phenothiazines 50 Epstein Barr virus EBV 50 basal cell nevus syndrome 50 DG# compounds targeting 50 AgRP 50 cisplatin resistant 50 promoter polymorphism 50 membranous nephritis 50 chemical malachite green 50 arthritis lupus 50 FANCD2 50 genetic defect 50 spokeswoman Christine Fanelle 50 mitochondrial metabolism 50 FMR1 gene 50 neurofibrillary 50 Toxoplasmosis 50 beta thalassemia 50 sporadic Creutzfeldt Jakob 50 Adenoviruses usually cause 50 IL 1Ra 50 APOE4 gene 50 thyrotropin levels 50 vaccine serotypes 50 NorStates Bank serves 50 prolonged immobilization 50 placenta praevia 50 Polycystic kidney disease 50 prostate bladder 50 Myocardial infarction 50 APOE 50 hypermethylation 50 ChR2 50 CYP #D# 50 antiphospholipid antibodies 50 chronic degenerative diseases 50 immunodeficiency disorder 50 serum BDNF 50 inverse agonist 50 COL#A# 50 inherited metabolic disorders 50 inhaled allergens 50 folic acid deficiency 50 ADAMTS# 50 systemic autoimmune 50 mutant gene 50 THEY SAY THE 50 Tor Bjerkedal report 50 non cirrhotic portal 50 Cowden syndrome 50 alpha thalassemia 50 Sudden infant 50 hyperandrogenism 50 adrenal suppression 50 CYP#B# 50 painful menstrual periods 50 hepatic renal 50 Acute Bacterial Sinusitis ABS 50 MTP inhibitor 50 capillary leak 50 hematopoietic cancers 50 prematurity ROP 50 micro RNAs 50 spontaneous mutations 50 SOX3 gene 50 chlamydial infection 50 beta carotene supplementation 50 CAG repeats 50 paroxetine sertraline 50 posing suffocation 50 subclinical hyperthyroidism 50 alpha defensin 50 g trans fats 50 NNRTI resistance 50 soluble tumor necrosis 50 facial clefts 50 transthyretin 50 IGF1 50 hereditary breast cancer 50 adenomatous polyps 50 miRNA genes 50 HMGA1 50 estrogen receptor alpha 50 Congenital heart 50 Tasigna prolongs 50 autosomal dominant 50 eczema hay fever 50 Genital herpes 50 ARID1A 50 MODY 50 neurodegenerative disorder characterized 50 immunopathology 49 Leukopenia neutropenia 49 nondemented 49 thyroid dysfunction 49 polycystic ovary 49 APOE genotype 49 ectopic expression 49 tumor suppressor gene 49 thalassemia trait 49 immunocompromised individuals 49 pheochromocytoma 49 nulliparous 49 inborn errors 49 GSTM1 gene 49 SLC#A# [001] 49 leptin receptors 49 inflammatory bowel syndrome 49 PPARg 49 GATA4 49 protein encoded 49 osteopenia osteoporosis 49 neurological abnormalities 49 Hereditary angioedema 49 G allele 49 prostate gland mammary gland 49 hyperplasia BPH 49 beta1 integrin 49 Pancreatic neuroendocrine tumors 49 Klinefelter syndrome 49 multivariate adjustment 49 Jhdm2a 49 Fanconi Anemia 49 Thyroid gland 49 IKZF1 49 #q# deletion syndrome 49 G6PD 49 predisposing factor 49 VLDL cholesterol 49 recessive gene 49 deacetylation 49 nicotine receptor 49 prostate cancer CaP 49 abnormal lipid 49 genetic mutation 49 genetically inherited 49 Iron deficiency anemia 49 Klotho gene 49 syndrome FXTAS 49 erythematosus 49 penile anal 49 adenocarcinomas 49 DISC1 gene 49 Mitochondrial diseases 49 gene APOE 49 prostate abnormalities 49 mRNA transcripts 49 prostate carcinogenesis 49 subfertility 49 Postmenopausal 49 paraneoplastic 49 TT genotype 49 mitochondrial disorders 49 inhibitory receptor 49 virulence genes 49 MIF gene 49 del 5q MDS 49 leptin resistant 49 hemoglobinopathies 49 NS5B polymerase 49 myeloproliferative 49 lipin 49 carotenoids flavonoids 49 J. Clin 49 ovarian hormones 49 Glioblastoma multiforme GBM 49 neuroblastomas 49 bronchopulmonary dysplasia 49 phyto oestrogens 49 severe obstructive pulmonary 49 infective agent 49 palladin 49 Folic Acid Supplements 49 TCF4 49 histone deacetylases 49 FMR1 49 Thromboembolic 49 diphtheria whooping cough tetanus 49 neoplasias 49 Chronic HCV 49 Pneumococcal pneumonia 49 Akt1 49 abnormal hemoglobin 49 murine leukemia virus 49 KCNQ1 49 apoE 49 JAK mutations 49 papillary renal cell carcinoma 49 CNTNAP2 49 progressive neurodegenerative 49 improves insulin sensitivity 49 Drug Prevents 49 Free Full Text 49 umol L 49 ectoderm 49 VKORC1 49 kidney allograft 49 Uncontrolled hypertension 49 mental retardation blindness 49 spontaneous mutation 49 GBA mutations 49 FGFs 49 autosomal dominant inheritance 49 fructose intolerance 49 Birth defects 49 motor neuron degeneration 49 Hurler syndrome 49 precancerous tumors 49 finasteride Proscar 49 Dysregulation 49 LDL receptor 49 pathogenic mutations 49 antiphospholipid syndrome 49 protein kinase C 49 FGFR2 gene 49 estrogen deficiency 49 5 hydroxytryptamine 49 varicella zoster virus 49 NSAID associated 49 TTR amyloidosis 49 penile cancers