Related by context. All words. (Click for frequent words.) 81 Meckel Gruber 63 Tay Sachs thalassemia 63 inherited mutations 62 recessive genetic disorders 61 chromosomal anomaly 61 clefting 61 cause cardiac channelopathies 60 BRAF gene mutations 60 Klinefelter syndrome 60 Becker muscular dystrophy 60 Kufs disease 60 WDR# 60 Hutchinson Gilford progeria 60 diabetes sciatica 60 Bardet Biedl syndrome 60 Epstein Barr Virus EBV 59 debilitating neurodegenerative disorder 59 fronto temporal dementia 59 spinal muscle atrophy 59 Celiac sprue 59 bought Glaxo Serevent 59 WAGR syndrome 59 Asperger syndrome milder 59 Childhood Disorder 59 LRRK2 gene 58 chromosome rearrangements 58 ORMDL3 58 causative gene 58 STK# gene 58 muscular dystrophy cystic fibrosis 58 By Peggy Bresnick 58 pediatrician Mensur 58 Polycystic ovarian syndrome 58 hypokalemia hypomagnesemia 58 cardiovascular restenosis cancer 58 phthalate syndrome 58 aneuploidies 58 Limperopoulos 58 MYH9 gene 58 hereditary spastic paraplegia 58 Crigler Najjar syndrome 58 neurobiological disorder 58 dyskeratosis congenita 58 CHD7 58 causative mutations 58 kidney urologic 58 congenital toxoplasmosis 58 Karayiorgou 58 TCF#L# gene 58 TTR amyloidosis 58 autosomal recessive 57 SHANK3 gene 57 Enrique Naputi 57 IDs Digal 57 chronic progressive neurodegenerative 57 Spinal muscular atrophy 57 Arrhythmogenic 57 deafness neurological 57 CDH1 57 Apert syndrome 57 PKU genetic 57 DNA methylation patterns 57 hereditary nonpolyposis colon cancer 57 preeclampsia gestational diabetes 57 underlying molecular mechanisms 57 Lafora disease 57 genes predisposing 57 HNPCC 57 autosomal recessive disease 57 chromosomal anomalies 57 Fragile X gene 57 occipital regions 57 neuro degenerative 57 Muscular dystrophies 57 IgA deficiency 57 hereditary nonpolyposis colorectal cancer 57 LIS1 57 included exfoliative dermatitis 57 genomewide association study 56 dysbindin gene 56 Jonathan Sebat 56 alpha1 antitrypsin deficiency 56 HGPS 56 Antisocial personality 56 Li Huei Tsai 56 pharynx larynx 56 neurodevelopment disorder 56 Teresa Graedon Ph.D. 56 Ribavirin causes 56 holoprosencephaly 56 channelopathies 56 sickle cell cystic fibrosis 56 VHL gene 56 Ardent Tillers 56 nonhereditary 56 heritable diseases 56 microdeletions 56 archaic ungulates 56 lissencephaly 56 prenatally diagnosed 56 TP# mutation 56 LMNA 56 ceroid lipofuscinosis NCL 56 dominantly inherited 56 developmental abnormalities 56 ovarian endometrial 56 Alport syndrome 56 anaphylactic reactions bronchospasm 56 severe congenital neutropenia 56 chronic lymphocytic 56 #:#-#,# CrossRef Medline [001] 56 achromatopsia 56 1 diabetes T1D 56 epigenetic regulation 56 bronchopulmonary dysplasia BPD 56 Dr. Bezprozvanny 56 autosomal recessive disorder 56 epigenetic changes 56 neurogenetic 56 Nonalcoholic fatty liver 56 Wolf Hirschhorn 56 vascular occlusive diseases 56 hereditary deafness 56 Li Fraumeni syndrome 56 auditory neuropathy 56 polymorphic ventricular tachycardia 56 apolipoprotein E4 56 childhood disintegrative disorder 56 Angelman syndrome 55 RUNX3 55 #q# deletion 55 biofilm formation dispersal 55 autosomal recessive genetic 55 ARID1A 55 non polyposis colorectal 55 neurodegenerative disorder characterized 55 hypermethylated 55 Rh factor 55 inherit predisposition 55 Fanconi Anemia 55 mitochondrial disorders 55 narcolepsy cataplexy 55 genetic syndromes 55 monogenic diabetes 55 Waqar Hussain Aman Yemer 55 myocardial infarction ventricular fibrillation 55 progranulin mutations 55 multisystem disease 55 Sixteen mummies 55 Max Delbruck Center 55 neurogenetics 55 GnT 4a 55 Alagille syndrome 55 Rubinstein Taybi syndrome 55 familial pancreatic cancer 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 neuropsychiatric illnesses 55 bone marrow mesenchymal stem 55 GPC5 55 chromosomal defect 55 MassGeneral Institute 55 Neurofibromatosis type 55 TACI mutations 55 ABCB1 55 MECP2 gene 55 DEC2 55 Brugada syndrome 55 APOL1 55 autoimmune thyroid 55 Hurler syndrome 55 Uterine cancer 55 Thomas Jessell 55 Von Willebrand disease 55 JAK mutations 55 neuronal precursor 55 Genetic variations 55 maternally inherited 55 Rb gene 55 VCFS 55 PLX STROKE targeting 55 genetic locus 55 heritable disorders 55 cystic fibrosis chronic pancreatitis 55 congenital disorders 55 precaution Wiehle 55 de novo mutations 55 neuropsychiatric disorder 55 progressive neurodegenerative 55 glutamic acid decarboxylase 55 sporadic Creutzfeldt Jakob 55 proband 55 wrote Anders Sundstrom 55 J. Biol 55 Heidi Rehm 55 Guoping Feng 55 cystic fibrosis muscular dystrophy 55 Derek Besenfelder 55 genetic variants associated 55 Vargha Khadem 55 Goltz syndrome 55 Bardet Biedl Syndrome 55 overt hepatic encephalopathy HE 55 Nahum Sonenberg 55 somatic mutations 55 hereditary predisposition 55 inhaled fibers 55 BY EDWARD ZERIN 55 Ets2 55 immunodeficiencies 55 neurofibrillary 55 fibrodysplasia ossificans progressiva FOP 55 microdeletion 55 mosaicism 54 autosomal dominant polycystic kidney 54 Cessna #R dual 54 autoimmune encephalitis 54 Osteogenesis imperfecta 54 Smith Lemli Opitz syndrome 54 mental retardation epilepsy 54 transfusion syndrome 54 untreated hypothyroidism 54 AAT deficiency 54 Joubert syndrome 54 remains mystery Yairi 54 antiphospholipid syndrome 54 Maven Semantic 54 embryonic germ 54 AML MDS 54 Cryptococcus neoformans 54 fatal neurodegenerative 54 Cowden syndrome 54 gene MECP2 54 murine leukemia virus 54 implicated Jessie Dotson 54 Waqar Hussain Aman Yamar 54 underlying pathophysiology 54 microcephalin 54 MSH2 54 neurexins 54 Suicidal tendencies 54 primary ciliary dyskinesia 54 non syndromic 54 inherited neurodegenerative 54 aneuploid cells 54 NPHP 54 NF1 54 Hashimoto thyroiditis 54 familial adenomatous polyposis FAP 54 mitochondrial dysfunction 54 common disabling neurological 54 homozygous FH 54 Fanconi anemia FA 54 opsoclonus myoclonus syndrome 54 Marou Awanis born 54 chromosomal abnormalities 54 primordial germ cells 54 Pancreatic insufficiency 54 dilated cardiomyopathy DCM 54 Cathy Wos contributed 54 Genetic Disorders 54 fetal chromosomal abnormalities 54 J. Dryden Kusar 54 progressive neurodegenerative disorder 54 chromosomal disorders 54 positional cloning 54 myopathies 54 mechanotransduction 54 thoracic aortic disease 54 LRP5 54 HHMI investigator 54 incurable genetic 54 Südhof 54 Velculescu 54 HBV HCV 54 asthma rheumatoid arthritis 54 genetic defects 54 Professor Woo Suk 54 chromosome abnormalities 54 genomic rearrangements 54 By Karen Pallarito 54 genus Plasmodium 54 NOMID 54 Long beaked Echidna 54 chromosomal translocations 54 non coding RNA 54 mitochondrial mutations 54 Genetic variants 54 Yuma grower 54 SEQureDx ™ 54 neurological disorder affecting 54 FTLD 54 recessive trait 54 Darell Bigner 54 autoinflammatory diseases 54 Matsuzawa pioneer 54 Brugada Syndrome 54 ENPP1 54 PON1 activity 54 fatal neurodegenerative disorder 54 mitochondrial defects 54 motor neuron degeneration 54 #q#.# deletion syndrome 54 neuro developmental 54 RPE# 54 oral Janus kinase 54 chromosomal rearrangement 54 Physiology Seminar 54 hippocampal function 54 BRCA2 breast cancer 54 myotonic dystrophy 54 SOD1 gene 54 Ventricular Dysplasia 54 prostate gland mammary gland 54 endocrine diseases 54 chromosome abnormality 54 mutated gene 53 prion infections 53 Evidence Therapeutic 53 breast cancer genes BRCA1 53 alzheimer disease 53 Bronchopulmonary Dysplasia 53 Korsakoff syndrome 53 Rh incompatibility 53 Tuberous sclerosis 53 Premature Ovarian Failure 53 By Alan Mozes 53 NDOW wildlife 53 protein misfolding 53 Genetic mutations 53 chemistry microbiology immunology 53 Severe acne 53 degenerative neurological diseases 53 c KIT 53 Leber congenital amaurosis LCA 53 microbial pathogenesis 53 Ari Melnick 53 primary ovarian insufficiency 53 familial adenomatous polyposis 53 molecular abnormalities 53 ciliopathies 53 chronic granulomatous disease 53 cystic fibrosis Duchenne muscular 53 methylation patterns 53 Neural tube 53 CIN lesions pre 53 muscular dystrophies 53 mutated BRCA 53 disorders ASD 53 tumor subtype 53 chromosomal aberration 53 neuromuscular dysfunction 53 autosomal dominant disorder 53 Myrna Weissman 53 cloned primate 53 Premature menopause 53 chromosomal aberrations 53 genetic abnormality 53 renovascular hypertension 53 comorbid anxiety 53 MGH MIND 53 Current Author Addresses 53 nerve degeneration 53 Physiology Anatomy 53 pulmonary thromboembolism 53 MC4R gene 53 Smith Lemli Opitz 53 medullary bones 53 Immunobiology 53 grizzlies roam 53 coagulation abnormalities 53 fruitfly Drosophila 53 #S ribosomal RNA 53 Li Fraumeni 53 By Kathleen Doheny 53 AP Photo Alkis 53 deCODE AF TM 53 galactosemia 53 Genetic predisposition 53 behavioral neuroscientist 53 Pelvic inflammatory 53 molar pregnancy 53 MZ methodology 53 Dravet syndrome 53 Harold D. Stolovitch 53 disease Chronic Traumatic 53 differential gene expression 53 neural tube defect 53 mutated genes 53 APOE genotype 53 moyamoya 53 associated tremor ataxia 53 genetic defect 53 MECP2 53 monogenic disorders 53 mitochondrial DNA mtDNA 53 prematurity ROP 53 invasive secretory carcinoma 53 genomic imprinting 53 pseudonym Loai 53 LHRH receptor positive 53 Sabina Sirny 53 Froguel 53 Lymphocytic 53 Meckel Gruber syndrome 53 Fanconi anemia 53 Prenatal diagnosis 53 inhibiting ovulation 53 vitro maturation 53 Angiograms carry slight 53 vWD 53 MLH1 53 intracranial atherosclerosis 53 Max Delbrueck Center 53 filaggrin 53 leptin deficiency 53 infertility miscarriages 53 Hereditary angioedema HAE 53 ankyrin B 53 #:#-#,# CrossRef Medline [002] 53 variant angina 53 Medulloblastoma 53 Edith Cora Tietge 53 inborn errors 53 neuropsychiatric diseases 53 Thorough cooking kills 53 Rando Allikmets 53 Cystic fibrosis CF 53 John Marvin Becklin 53 inherited retinal degeneration 53 Postherpetic neuralgia 53 siRNA knockdown 53 Fetal alcohol 53 genetic imprinting 53 STAT4 53 Nickolas Papadopoulos 53 Sandhoff disease 53 Services #:#-#,# Abstract 53 #q# deletion syndrome 53 deCODE ProstateCancer TM 53 myelofibrosis polycythemia vera 53 autism susceptibility genes 53 hypertension cardiovascular disease 53 MD MHSc 53 TCF4 53 dopamine D4 receptor 53 DEAR1 53 coma convulsions 53 unknown etiology 53 cardiovascular endocrine 53 Congenital heart 53 shorter telomere length 53 CYP#A# CYP#D# 53 Andrew Feigin 53 rhinovirus infection 53 Autoimmune disorders 53 disorders Elekta Axesse 53 #q#.# [001] 53 MCAD deficiency 53 TomTom NAVIGATOR software 53 Mitochondrial diseases 53 KRAS oncogene 53 Aspiration pneumonia 53 FXTAS 53 Doron Behar 53 Dr. Honglei Chen 53 ovarian pancreatic 53 Leber hereditary optic neuropathy 53 AAT Deficiency 53 velo cardio facial 53 By Jeanne Ruczhak 53 Yamanaka recipe 53 Brd4 53 Maroteaux Lamy Syndrome 53 untreated STDs 53 CFTR gene 53 By EJ Mundell 53 epigenetic alterations 53 lysosomal storage disease 53 identify chromosomal translocation 53 polycystic ovarian disease 53 Cockayne syndrome 53 impaired insulin secretion 53 Moyamoya disease 53 TMEM#B 52 rheumatoid arthritis lupus 52 Alzheimer disease vascular dementia 52 undiagnosed celiac disease 52 genotoxic stress 52 severe dehydrating diarrhea 52 Comorbid 52 LQTS 52 By Steven Reinberg 52 Congenital Muscular Dystrophy 52 biologic pathways 52 spore forming bacterium Bacillus 52 Epstein Barr virus EBV 52 Pervasive Developmental Disorder 52 thrombophilia 52 Fatty Liver Clinic 52 detecting biochemical 52 perinatal complications 52 APOE gene 52 GLA def 52 MELAS 52 affective psychoses 52 Cognitive Neurology 52 generalized epilepsy 52 Sadaf Farooqi 52 clinically heterogeneous 52 PTPN# 52 completed postdoctoral fellowship 52 demonstrated anti amnesic 52 psoriasis inflammatory bowel 52 Jakob Disease 52 enterocolitis 52 By Vaneta Rogers 52 Helmholtz Zentrum Munchen 52 congenital deafness 52 genomewide 52 Staff Writer jeffd@nwanews.com 52 polycystic ovarian syndrome PCOS 52 Polycomb proteins 52 Generalized anxiety disorder 52 Fetal heartbeats 52 maintaining cardiorespiratory fitness 52 later Ettore Campogalliani 52 Juchen C. Martial 52 pre eclamptic 52 epigenetic inheritance 52 Ichiro Kawachi 52 retinitis pigmentosa degenerative 52 G6PD deficiency 52 Renata Pasqualini 52 spastic diplegia 52 Cognitive Problems 52 Epidermolysis bullosa 52 Peutz Jeghers syndrome 52 neuro developmental disorder 52 Karolinska Institutet Stockholm Sweden 52 BRCA1 mutations 52 Christos Mantzoros 52 unresectable tumors 52 MD ScD 52 Hypophosphatasia 52 pharmacogenomic translational research 52 Improper braking 52 pancreatic endocrine 52 IKZF1 52 susceptibility genes 52 onset sepsis 52 mouse mammary 52 PCA3 gene 52 trypanosome parasite 52 Neurovirology 52 monogenic 52 Functional neuroimaging 52 genetic rearrangements 52 galactose intolerance severe 52 CNTNAP2 52 Alimentary Tract 52 chaotic menstrual cycles 52 neurodevelopmental disorder 52 J Am Acad 52 Dtsch Arztebl Int 52 immunodeficiency disorder 52 lysosomal storage diseases 52 tryptase 52 By Ed Edelson 52 genetic determinants 52 diabetes mellitus autoimmune disorders 52 glycan microarray 52 Ehrlichia 52 Jaakko Kaprio 52 protein misfolding diseases 52 ambiguous genitalia 52 severe obstructive pulmonary 52 alexithymia 52 bacterium Mycobacterium tuberculosis 52 Polycystic ovary syndrome PCOS 52 neuromotor 52 genetic polymorphisms 52 #:# WHEATON substitution 52 telemonitoring imaging 52 previously uncharacterized 52 WRN gene 52 fatal myelination disorder 52 testicular germ cell 52 BRAF gene 52 Selenium deficiency 52 Georgi Lazov kneeling 52 Latrisha Fields Carruthers 52 dermatologic reactions 52 Fragile X Syndrome 52 Wai Lang 52 mother Zheng Yaru 52 Invasive pneumococcal disease 52 myeloproliferative neoplasms 52 inherited neurological disorder 52 genetic lysosomal storage 52 Neurodegenerative disorders 52 ADPKD 52 inherited metabolic disorders 52 fat malabsorption 52 MD Ph.D. Mayo Clinic 52 trap antimatter atoms 52 MD MSCE 52 arrhythmogenic right 52 Lafora 52 chromosomal deletions 52 splice junctions 52 makers Britains Heyde 52 Cinzia Marano 52 pelvic malignancies 52 Carolyn Edds 52 epilepsy cerebral palsy 52 McKusick Nathans Institute 52 gastroenteritis skin rashes 52 cystic fibrosis sickle cell 52 Oxidative damage 52 Alleles 52 EOquin TM phase 52 hyperinsulinism 52 Dr. Stacy Tessler 52 susceptibility gene 52 anterior pituitary 52 dopamine receptor gene 52 Bronchiolitis 52 congenital deficiency 52 BMPR2 52 Cerebral palsy involves 52 genetic loci 52 Klonoski suffered 52 Myocardial infarction 52 Molnar Szakacs 52 PTCHD1 gene 52 Grace Tallarico 52 FMR1 gene 52 retinoblastoma Rb 52 Treatment Shows Promise 52 LPA receptors 52 Yong Yen Nie 52 histone H4 52 Cedano Holyfield 4 52 Genetic Variation 52 Prion diseases 51 bacteria Neisseria meningitidis 51 hereditary pancreatitis 51 susceptibility locus 51 Retinitis pigmentosa 51 NPM1 gene 51 Tony Wyss Coray 51 Male infertility 51 skeletal muscle weakness 51 lymphomas leukemias 51 lichen planus 51 epigenetic mechanisms 51 Emma Hitt 51 NOTCH1 51 FGFs 51 PTEN gene 51 Editors Anand Krishnamoorthy 51 nongenetic factors 51 neuropathologic 51 ataxia telangiectasia 51 pathogenic mutations 51 persistent pulmonary hypertension 51 Duchenne muscular dystrophy DMD 51 naturally occurring neuroprotective 51 Streptococcus agalactiae 51 THE ASSOCIATED PRESS Katsumi 51 Polymorphic Ventricular Tachycardia CPVT 51 biochemical imbalances 51 medium chain acyl 51 Entamoeba histolytica 51 Bullous 51 By Wai Lang 51 Epstein Barr Virus 51 T1DM 51 Chronic ITP 51 epidermolysis bullosa EB 51 chromosomal imbalance 51 Beta thalassemia 51 recessively inherited 51 facial clefts 51 reproductive endocrine 51 juvenile idiopathic arthritis 51 DMSc 51 Cancer Incidence Mortality 51 Developmental Genetics 51 Angela Genge 51 anesthesia neuroanatomy obstetrics 51 Globe Correspondent #/#/# [002] 51 PTEN tumor suppressor 51 unmeasured factors 51 MTHFR 51 Hyperthyroidism 51 Wiskott Aldrich Syndrome 51 ataxias 51 amyloid cascade 51 cybertheft cyberfraud cyberwarfare 51 mastocytosis 51 Joshua Schier 51 Gina Partington 51 Shumyatsky 51 COMT gene 51 condition Arrhythmogenic Right 51 germline mutations 51 sporadic ALS 51 retinal dysfunction 51 ectodermal dysplasia 51 John M Grohol 51 medulloblastomas 51 Klinefelter Syndrome 51 recessive inheritance 51 Kim Raum Suryan 51 bicuspid valve 51 proliferative retinopathy 51 Cockayne Syndrome 51 FASPS 51 Azim Surani professor 51 Braunwald E 51 myelomeningocele 51 Schieffer chuckled 51 About Rigel Rigel 51 DVM PhD Dipl 51 Patau syndrome 51 cardiac channelopathies 51 Cardiovascular Epidemiology 51 dysgenesis 51 CMV infections 51 Jacques Donnez 51 either ischemic clog 51 neuropsychiatric disorders 51 DICER1 gene 51 Linda Calabresi 51 multiprotein complex 51 CRIMSON STAFF WRITER 51 Tasigna prolongs 51 genetic neuromuscular disorder 51 highly heritable 51 papillary renal cell carcinoma 51 C1 INH deficiency 51 genetic abnormalities 51 Spokeswoman Whitney Jodry 51 molecular virology immunology 51 Dysplasia 51 biochemical abnormalities 51 Neil Scolding 51 genetically mapped 51 Margaret Honein 51 octuplets conceived 51 KIBRA 51 Ibrahim Abdel Qader 51 neurobiological disorders 51 Apr RSV# 51 Igor Grigoriev 51 pseudotumor cerebri 51 intestinal microbiota 51 myelogenous leukemia 51 hormonal disorders 51 primary biliary cirrhosis 51 MAP kinases 51 Jannelle Cintron 4 51 hydrops 51 Bartonella species 51 Peter Itin 51 #-month/#-month Aug [002] 51 genes encode proteins 51 arsenic sulfide 51 heritable genetic 51 Country singer Tompall 51 GFP gene 51 Dr. Helen Lavretsky 51 Marcelo Reales 51 vasa previa 51 CNVs 51 Lynda Chin 51 susceptibility loci 51 Adrenoleukodystrophy 51 Karolinska Institute Stockholm 51 Alcoholism COGA 51 polycystic ovary 51 physiological nutritional 51 serum leptin 51 inappropriate antidiuretic hormone SIADH 51 Levy Lahad 51 familial aggregation 51 congenital cataract 51 unexplained infertility 51 hamartomas 51 Dr. Loeken 51 Multivariable logistic regression 51 chronically immunosuppressed solid 51 Sven Cnattingius 51 limb deformities 51 spastic paraplegia 51 disorder FASD 51 Neurogenetics 51 Neurological disorders 51 Christiane Reitz 51 Systemic lupus erythematosus SLE 51 Von Hippel Lindau 51 long QT syndrome 51 Molly Thornberg 51 Ultrasonographic 51 Matthew Meyerson 51 Milan Hayat Stapp 51 parkin gene 51 Proteus syndrome 51 Karolinska Institutet Sweden 51 Pier Paolo Pandolfi 51 inheritable diseases 51 Rhesus disease 51 Severe Combined Immunodeficiency 51 nonsense mutations 51 autistic traits 51 PON1 51 Ina Caterina Remhof 51 molecular mechanisms underlying 51 Am J Geriatr 51 Preimplantation genetic diagnosis 51 endocrine disorder 51 hemolytic disease 51 prostate carcinogenesis 51 Ann Graybiel 51 neuro degenerative disorders 51 neuroD2 51 androgen receptor gene 51 stepgrandchild 51 chromosomal regions 51 Lisa DeBruine 51 interferon pathway 51 Imprinted genes 51 WiseAnalytics Lyndsay Wise 51 Henoch purpura 51 MeCP2 protein 51 Phenylketonuria PKU 51 DICER1 51 APOE e4 51 relapsed ALL 51 Prevotella 51 xenotropic murine leukemia 51 chronic autoimmune disorder 51 fibrodysplasia ossificans progressiva 51 Vascular dementia 51 Aspergers Syndrome 51 progressive retinal degenerative 51 YL Kao ENDITEM J 51 6/lf 51 neural degeneration 51 By Seo Jee 51 folate vitamin B6 51 NF2 51 Porphyria 51 meningitis encephalitis 51 temporomandibular joint syndrome 51 Koenekoop 51 idiopathic pulmonary 51 Chlamydophila pneumoniae 51 leukodystrophies 51 epigenetic silencing 51 Cell Mol Physiol 50 asthma rhinitis 50 autosomal dominant 50 Colon polyps 50 Pneumococcal pneumonia 50 transformed peptic ulcer 50 paternally inherited 50 Sociodemographic 50 inherited retinal 50 Hypertensive heart 50 incurable neurological disorder 50 Myotonic dystrophy 50 Shrikant Mane 50 Titus Ernstoff 50 untreated sleep apnea 50 Ga Woon Philip Vahn 50 Tim Lambert deltoidblog 50 Sacktor 50 Centers Helmholtz Gemeinschaft 50 bladder exstrophy 50 polydactylism 50 lipoprotein metabolism 50 serotonin transporters 50 Neurodegenerative diseases 50 Blanchette Hooker 50 Simin Nikbin Meydani 50 RRM1 50 mammary cells 50 autoinflammatory 50 epigenetic modification 50 biliary atresia rare 50 number NCT# ClinicalTrials.gov 50 metachromatic leukodystrophy 50 Marten Hans 50 UGT#A# * 50 Victor Velculescu 50 BRCA2 carriers 50 Seeking LPN 50 http:/www.qiagen.com/ 50 Congenital Adrenal Hyperplasia 50 Stuttering tends 50 pathogenetic mechanisms 50 Alport Syndrome 50 postnatally 50 Villejuif France 50 apolipoprotein E gene 50 familial hypercholesterolemia 50 Neurodegenerative Disorders 50 Fragile X syndrome 50 Thyroid disorders 50 pancreatic prostate 50 nongenetic 50 cerebral palsy Down syndrome 50 Blackburn Greider 50 lupus scleroderma 50 thyroid deficiency 50 Lesch Nyhan syndrome 50 Shrinivas Kulkarni 50 Loeys Dietz syndrome 50 Laugeson 50 Neuropsychiatric Genetics 50 neurodevelopmental disorders 50 Mouse Models 50 INSPIRE Trial Phase III 50 selectively modulating 50 untreated obstructive sleep 50 Progenitor cells 50 Sina Bavari 50 synaptic function 50 diaphragmatic hernia 50 Heterozygous 50 obstructive coronary 50 deformed fetuses dying 50 subclinical disease 50 fetal chromosomal 50 immuno compromised individuals 50 chromosome #q#.# [001] 50 Polycystic Ovary Syndrome 50 neurobehavioral disorder 50 serratia 50 Dr. Rochelle Dicker 50 neurocognitive dysfunction 50 Premature Aging 50 Polycystic Ovarian Syndrome PCOS 50 GERD migraine headaches 50 Pak Michele Redman 50 Wiskott Aldrich syndrome 50 MD D.Sc. 50 Myocarditis 50 hip osteonecrosis avascular 50 incurable degenerative 50 myelodysplasia 50 spina bifida cerebral palsy 50 observable traits 50 DiGeorge syndrome 50 Sudha Seshadri MD 50 High Functioning Autism 50 Mathias Treier 50 neuro developmental disorders 50 shortened telomeres 50 recessive genetic 50 FMR1 50 neuroinflammation 50 gestational diabetes mellitus 50 MD DMSc 50 G#S mutation 50 Universitätsklinikum 50 Radiographic findings 50 Trichomonas vaginalis 50 subtyped 50 skin ligaments tendons 50 cryptococcal meningitis 50 vascular endothelial dysfunction 50 bronchopulmonary dysplasia 50 folate metabolism 50 Lisa Mosconi 50 Hirschsprung disease 50 monozygotic 50 Tuberous Sclerosis Complex 50 postoperative delirium 50 retinitis pigmentosa RP 50 Coeliac disease 50 Maroteaux Lamy syndrome 50 granulosa cell 50 PCR RFLP 50 aspergillosis candidiasis coccidioidomycosis listeIRF6 gene 50 MYH9 50 Mantzoros 50 hyper IgE syndrome 50 stroke hypertension palpitations 50 Wnt#b 50 mutations 50 pathophysiological effects 50 Autistic Spectrum Disorders 50 J Am Coll 50 genomic alterations 50 Arch Surg 50 Heterozygous Familial Hypercholesterolemia