Related by context. All words. (Click for frequent words.) 57 SCA5 55 dyskeratosis congenita 55 fatal neuromuscular disorder 54 spontaneous remission 54 holoprosencephaly 53 MGUS 53 Leber hereditary optic neuropathy 53 chromosome abnormality 53 neurodegenerative disorder 53 Hashimoto thyroiditis 53 familial ALS 53 nonhereditary 53 Vitamin B# deficiency 52 Lafora disease 52 alexia 52 Cockayne syndrome 52 inherited neurological disorder 52 generalized epilepsy 51 AAT deficiency 51 hereditary hemochromatosis 51 progressive neurodegenerative disorder 51 Dilated cardiomyopathy 51 prosopagnosia 51 genetic abnormality 51 immunodeficiencies 51 autosomal dominant disorder 51 Myasthenia gravis 51 nongenetic 51 Hutchinson Gilford progeria 51 ADPKD 51 Brugada syndrome 51 systemic amyloidosis 51 genetic neuromuscular disorder 50 variable immunodeficiency 50 Chronic pancreatitis 50 autosomal dominant 50 FASPS 50 #q#.# deletion syndrome 50 untreated celiac disease 50 HUMIRA resembles antibodies 50 lichen planus 50 ectodermal dysplasia 50 idiopathic epilepsy 50 hereditary spastic paraplegia 50 multisystem disease 50 Male pattern baldness 50 WAGR syndrome 50 pernicious anemia 50 Chiari malformation 50 Malignant mesothelioma 50 recessive inheritance 50 autosomal recessive 50 Pernicious anemia 50 Raynaud disease 50 dominantly inherited 50 Hypophosphatasia 50 Pulmonary hypertension 50 polydactylism 50 Marfan syndrome 50 systemic scleroderma 49 MYH9 gene 49 gene APOE4 49 paraganglioma 49 neuropsychiatric disorder 49 degenerative neurological disease 49 myalgic encephalomyelitis ME 49 TACI mutations 49 neurofibromas 49 spinal muscle atrophy 49 Polycystic kidney disease 49 Dravet syndrome 49 fronto temporal dementia 49 hereditary predisposition 49 underlying pathophysiology 49 Von Willebrand disease 49 TP# mutation 49 endocrine disorder 49 Myotonic dystrophy 49 fatal neurodegenerative 49 genetic syndromes 49 hereditary degenerative 49 roseola 49 genomic variants 49 autosomal recessive disease 49 Mental retardation 49 Autoimmune diseases 49 lateral sclerosis ALS 49 fatal neurodegenerative disorder 49 HNPCC 49 Klinefelter syndrome 49 recessive trait 49 pathophysiologic 48 Motor neurone disease 48 Angelman syndrome 48 Coeliac disease 48 dementia praecox 48 Vascular dementia 48 myelodysplasia 48 incurable genetic 48 Shy Drager syndrome 48 monogenic 48 Diverticulosis 48 Hypertrophic cardiomyopathy 48 spontaneous mutation 48 de novo mutations 48 myotonic dystrophy 48 FTLD 48 Irritable bowel syndrome 48 Rh factor 48 basal cell nevus syndrome 48 benign positional vertigo 48 autosomal recessive genetic 48 neurasthenia 48 Pelizaeus Merzbacher disease 48 familial pancreatic cancer 48 Great Imitator 48 Fatty liver 48 Myelodysplastic syndrome 48 inherited retinal degeneration 48 Ischaemic heart 48 genetically inherited 47 embryonal rhabdomyosarcoma 47 Churg Strauss syndrome 47 Leber congenital amaurosis LCA 47 Kufs disease 47 susceptibility gene 47 lysosomal storage disease 47 cortical dysplasia 47 autoinflammatory diseases 47 APOE4 47 frontotemporal dementia 47 Aortic stenosis 47 Atopic dermatitis 47 sporadic Creutzfeldt Jakob 47 degenerative neurological disorder 47 Mendelian disorders 47 Osteogenesis imperfecta 47 Wiskott Aldrich Syndrome 47 spinocerebellar ataxia 47 inherited mutations 47 chromosome deletion 47 savant syndrome 47 dysgenesis 47 familial aggregation 47 thyroid dysfunction 47 Canavan Disease 47 Hutchinson Gilford Progeria Syndrome 47 Myocarditis 47 mitochondrial disease 47 acute rheumatic fever 47 huntingtin gene 47 auditory neuropathy 47 subclinical hyperthyroidism 47 fibrodysplasia ossificans progressiva FOP 47 skeletal dysplasia 47 Arnold Chiari Malformation 47 IgA deficiency 47 recessive genetic 47 inherited genetic mutations 47 juvenile myelomonocytic leukemia 47 HFE gene 47 Brugada Syndrome 47 Lennox Gastaut syndrome 47 pseudotumor cerebri 47 hydrops 47 apolipoprotein E gene 47 spontaneous mutations 47 subclinical 47 Endometrial cancer 47 Neurofibromatosis type 47 porphyria 47 sporadic ALS 47 incurable neurodegenerative disease 47 Genetic predisposition 47 Dental fluorosis 46 Systemic lupus erythematosus 46 Genetic mutation 46 inherit predisposition 46 degenerative neurological condition 46 hereditary deafness 46 Zinc deficiency 46 sweats excessively 46 multisystem disorder 46 degenerative neuromuscular disease 46 progressive neurodegenerative disorders 46 hypertrophic cardiomyopathy HCM 46 Spinal muscular atrophy 46 Diamond Blackfan anemia 46 GBA mutations 46 antithrombin deficiency 46 brain malformation 46 phobia neophobia 46 Tay Sachs thalassemia 46 ApoE4 46 APOE ε4 46 Joubert syndrome 46 incurable neurological disorder 46 APOE gene 46 TTR amyloidosis 46 degenerative disorder 46 Crigler Najjar syndrome 46 periodontal infection 46 Proteus syndrome 46 hyperinsulinism 46 sCJD 46 AAT Deficiency 46 fat malabsorption 46 neurodevelopmental disorder 46 ataxias 46 G#S mutation 46 multiple sclerosis lupus 46 leptin deficiency 46 essential thrombocythemia 46 Tourette syndrome neurological disorder 46 lactose malabsorption 46 Insulin resistance 46 hemochromatosis 46 recessively inherited 46 axonal damage 46 progressive neurodegenerative 46 degenerative nerve disorder 46 autoimmune pancreatitis 46 LRRK2 gene 46 Schizoaffective disorder 46 allelic variants 46 chronic autoimmune disorder 46 chromosomal imbalance 46 chromosomal anomaly 46 atypical parkinsonism 46 neurologic disorder 46 hereditary blindness 46 heterotaxy 46 Hirschsprung disease 46 autoimmune thyroiditis 46 Parkinson degenerative 46 Epileptic seizures 46 Essential tremor 46 Hurler syndrome 46 syringomyelia 46 missense mutations 46 exfoliation glaucoma 46 vascular Ehlers Danlos 46 DiGeorge syndrome 46 temporal arteritis 46 Ectopia Cordis 45 haemochromatosis 45 Hyperthyroidism 45 monoclonal gammopathy 45 progressive neurodegenerative disease 45 penetrance 45 neuro degenerative disorder 45 MSH2 45 NPM1 gene 45 hippocampal function 45 Cystic fibrosis CF 45 unprovoked seizures 45 CCR5 delta# 45 myeloproliferative 45 DiGeorge Syndrome 45 dissociative amnesia 45 LRRK2 mutations 45 TCF#L# gene 45 Muscular dystrophy 45 causative gene 45 super spreaders 45 peptic ulcer disease 45 Joubert Syndrome 45 NF1 45 Arrhythmogenic Right Ventricular Cardiomyopathy 45 neurological disorder affecting 45 Pulmonary arterial hypertension 45 CDH1 45 autonomic dysfunction 45 disabling neurological 45 chromosomal disorder 45 alpha thalassemia 45 Alopecia areata 45 inherited predisposition 45 bronchogenic carcinoma 45 germline mutations 45 neurological abnormalities 45 polymyalgia 45 MYH9 45 autosomal recessive disorder 45 PNET 45 microcephaly 45 VHL gene 45 aetiological 45 rare chromosomal disorder 45 congenital muscular dystrophy 45 Dwarfism 45 Long QT syndrome 45 Hemochromatosis 45 eosinophilic 45 Fanconi anemia 45 Mitral regurgitation 45 paraneoplastic 45 neurodevelopment disorder 45 chromosomal alterations 45 malignant transformation 45 neoplasias 45 maternally inherited 45 epididymitis 45 Osteogenesis Imperfecta 45 meningitis encephalitis 45 benign proliferative breast 45 childhood disintegrative disorder 45 Hurthle cell 45 Six3 45 predisposing factor 45 familial hypercholesterolemia 45 chromosomal disorders 45 paragangliomas 45 GSTM1 gene 45 lactase deficiency 45 sickle cell cystic fibrosis 45 malignant hyperthermia 45 Crouzon Syndrome 45 Li Fraumeni syndrome 45 Anencephaly 45 nondemented 45 genes predisposing 45 recurrent miscarriages 45 JAK2 mutation 45 Genetic variants 45 genetic lysosomal storage 45 myeloproliferative neoplasms 45 discoid lupus 45 hormonal disorder 45 pulmonary hypertension PH 45 proband 44 Leber congenital amaurosis 44 Chronic inflammation 44 McCune Albright 44 chromosomal rearrangement 44 Severe Combined Immunodeficiency 44 systemic mastocytosis 44 rheumatic disease 44 nerve degeneration 44 polydactyly 44 Parkinson disease degenerative neurological 44 imperfecta 44 Retinitis pigmentosa 44 Colorectal cancers 44 systemic autoimmune 44 Alport syndrome 44 progranulin gene 44 spastic diplegia 44 nonsense mutations 44 defective gene 44 Reye syndrome 44 Marfan syndrome genetic 44 Sarcopenia 44 bicuspid valve 44 achondroplasia 44 microdeletion 44 G#S [002] 44 neurodegenerative disorder characterized 44 paroxysmal nocturnal hemoglobinuria 44 hypogonadotropic hypogonadism 44 gene mutations 44 Cowden syndrome 44 Ovary removal 44 Androgenetic alopecia 44 mosaicism 44 pheochromocytoma 44 androgenetic alopecia 44 ApoE gene 44 familial adenomatous polyposis FAP 44 LHON 44 enterocolitis 44 Excessive sweating 44 Stumbrys 44 Loeys Dietz syndrome 44 Vitamin D insufficiency 44 Inflammatory bowel disease 44 thalassemia sickle cell 44 hypochondriasis 44 ichthyosis 44 cardiac fibrosis 44 chromosomal deletions 44 diabetes insipidus 44 classic autism Asperger 44 alveolar rhabdomyosarcoma 44 muscular dystrophy cystic fibrosis 44 COMT gene 44 Spina bifida 44 Hutchinson Gilford Progeria 44 familial adenomatous polyposis 44 primary progressive aphasia 44 FXTAS 44 autoinflammatory 44 APOE e4 44 induced cardiomyopathy 44 Y chromosomal 44 anatomical abnormalities 44 mitochondrial mutations 44 progressive degenerative neurological 44 PTEN mutations 44 mitochondrial disorders 44 Peripheral neuropathy 44 parkinsonism 44 mental retardation epilepsy 44 ApoE4 gene 44 myeloproliferative neoplasms MPNs 44 Congenital Adrenal Hyperplasia 43 primary ciliary dyskinesia 43 neurofibroma 43 nephrosis 43 ventricular cardiomyopathy 43 testicular tumors 43 breast cancer genes BRCA1 43 gene p# 43 multi infarct dementia 43 hyperinsulinemia 43 causative genes 43 CHD7 43 retinitis pigmentosa RP 43 promyelocytic leukemia 43 GSTT1 43 microdeletions 43 metaplasia 43 channelopathies 43 chromosomal anomalies 43 RDEB 43 biphosphonates 43 pheochromocytomas 43 hereditary pancreatitis 43 Meckel Gruber 43 progressive degenerative 43 non polyposis colorectal 43 autosomal 43 MECP2 gene 43 pyloric stenosis 43 VCFS 43 Aicardi syndrome 43 clinically heterogeneous 43 Heredity 43 mtDNA mutations 43 Sjögren syndrome 43 iCrime Wave begins 43 polygenic 43 Tay Sachs disease 43 Dave Chapelle skit 43 cerebri 43 McCOOK LAKE SD KTIV 43 Radiographic findings 43 facioscapulohumeral muscular dystrophy 43 situs inversus 43 chromosomal instability 43 Krabbe leukodystrophy 43 Hypertrophic 43 Epidermolysis bullosa 43 Lou Gherig Disease 43 beta thalassemia 43 water soluble vitamin 43 skeletal fluorosis 43 STK# gene 43 Peutz Jeghers syndrome 43 neurological manifestations 43 intestinal ulcers 43 factitious disorder 43 Fragile X gene 43 cystic fibrosis chronic pancreatitis 43 cryptogenic 43 idiopathic 43 V Leiden 43 nephritis 43 genetic disorder 43 Dental caries 43 vascular cognitive impairment 43 cardiac insufficiency 43 somatic mutation 43 Flu epidemics 43 Usher Syndrome 43 #q#.# [001] 43 progressive neurological disorder 42 spastic colon 42 familial clustering 42 Wolf Hirschhorn 42 hepatotoxic 42 aneuploidies 42 susceptibility genes 42 Retinoblastoma 42 amyloidosis 42 XMRV infection 42 Shwachman Diamond Syndrome 42 mutated genes 42 ataxia 42 angular cheilitis 42 Chronic fatigue 42 metabolic disorder 42 osteopetrosis 42 Mitochondrial dysfunction 42 Huntingtin 42 autoimmune thyroid 42 aciduria 42 teratogens 42 blood clotting disorder 42 neuro degenerative 42 BRCA mutation 42 bacteria Helicobacter pylori 42 Wilms Tumor 42 germline mutation 42 myoclonic epilepsy 42 epigenetic changes 42 spastic paraplegia 42 myocarditis inflammation 42 progressive degeneration 42 epidermolysis bullosa EB 42 motor neuron diseases 42 Leber Congenital Amaurosis LCA 42 chronic rheumatic 42 intersexuality 42 Periodontal disease 42 Krabbe Leukodystrophy 42 klotho 42 monogenic diabetes 42 Retinitis Pigmentosa RP 42 Ehlers Danlos syndrome 42 Krabbe Disease 42 Sickle cell 42 underactive thyroid gland 42 familial hypercholesterolemia FH 42 microscopic colitis 42 nonprogressive 42 FSGS 42 arthrogryposis 42 entering Triv 42 APOE genotype 42 HLA DRB1 42 bicuspid aortic valve 42 genes encode proteins 42 renal fibrosis 42 genetic alterations 42 neurobiological disorder 42 CFTR gene 42 inherited neurodegenerative 42 degenerative neurological 42 hereditary disorders 42 genomic instability 42 abnormal glucose metabolism 42 genetic defect 42 coprolalia 42 Beta thalassemia 42 SHANK3 gene 42 genetic susceptibility 42 atherosclerotic cardiovascular disease 42 mutation 42 incurable degenerative 42 Barrett esophagus 42 genes predispose 42 gene locus 42 disease NAFLD 42 benign polyps 42 extra centrosomes 42 aniridia 42 neonatal lupus 42 blindness paralysis 42 autosomal dominant polycystic kidney 42 multigenic 41 Moebius syndrome 41 pattern baldness 41 mutated gene 41 achromatopsia 41 interstitial nephritis 41 Telomere length 41 shorter telomeres 41 Oxidative stress 41 hyperparathyroidism 41 G6PD deficiency 41 testicular germ cell 41 cataracts clouding 41 lissencephaly 41 embryonal 41 ORMDL3 41 chromosomal defects 41 pilocytic astrocytomas 41 intestinal polyps 41 hypokalemia hypomagnesemia 41 cause cardiac channelopathies 41 Hereditary angioedema 41 nutritional deficiency 41 multifactorial 41 pyelonephritis 41 p# mutations 41 NF1 gene 41 obstructive coronary 41 onset Alzheimer 41 vindictiveness Osborne 41 retinal dysfunction 41 Stargardt Macular Dystrophy 41 hepatitis B infection 41 Henoch purpura 41 shaking palsy 41 hyperemesis gravidarum 41 chronicity 41 clotting disorder 41 recessive gene 41 Parkinson disease degenerative 41 CHARGE syndrome 41 Sjogren Syndrome 41 gene mutation 41 von Hippel Lindau 41 Rubinstein Taybi syndrome 41 PTEN gene 41 amenorrhoea 41 heritable 41 ARVC 41 proliferative diabetic retinopathy 41 filaggrin 41 motor neurone 41 diffuse gastric 41 Hip dysplasia 41 congenital anomaly 41 hypercoagulability 41 independents racial stereotyping 41 premature senility 41 #p#.# [001] 41 polyploidy 41 Li Fraumeni 41 primary sclerosing cholangitis 41 genetic abnormalities 41 Hirschsprung Disease 41 neural crest 41 bones Lyson 41 Crouzon syndrome 41 square jawed graduate 41 cerebellar ataxia 41 Indonesians Suharto 41 polymyositis 41 celiac sprue 41 primary biliary cirrhosis 41 septo optic dysplasia 41 Mendelian diseases 41 phenotypic variation 41 Corn Snow CORN 41 premalignant 40 Von Hippel Lindau 40 PALB2 40 traumatic disabling neurological 40 Maroteaux Lamy Syndrome 40 erythema nodosum 40 Tension headaches 40 hypertrichosis 40 pathognomonic 40 tricuspid atresia 40 autosomal dominant inheritance 40 Bed wetting 40 debilitating neurodegenerative 40 neoplasm 40 viral etiology 40 Mendelian 40 velo cardio facial 40 5q 40 chronic obstructive airway 40 neoplastic 40 gene variant 40 Apert syndrome 40 motor neuron disease 40 Fragile X Syndrome 40 hereditary nonpolyposis colorectal cancer 40 Telomere shortening 40 Raynaud syndrome 40 galactose intolerance severe 40 Parkinsons disease 40 polycystic ovary syndrome 40 opsoclonus myoclonus syndrome 40 Oppositional Defiant Disorder 40 leukodystrophies 40 IKZF1 40 cardiac channelopathies 40 cystic fibrosis Duchenne muscular 40 BRCA2 gene 40 congential 40 highly heritable 40 neurogenic 40 SCN9A gene 40 rearview mirror Dworaczyk joked 40 macular disease 40 filaggrin gene 40 chromosomal rearrangements 40 hereditary disorder 40 ocular albinism 40 phenotypic expression 40 ABO blood 40 neurologic deficits 40 genomic imprinting 40 cardiac arrythmia 40 CYP#A# gene 40 ADA SCID 40 genes BRCA1 40 Benign breast 40 gastric atrophy 40 micro RNAs 40 arteriosclerotic 40 Frontal lobe 40 hereditary hemorrhagic telangiectasia 40 hypoplastic 40 primitive neuroectodermal tumor 40 Th2 cells 40 monozygotic twins 40 premature ovarian 40 familial polyposis 40 corneal dystrophy 40 F. necrophorum 40 Xingu River rises 40 subtype 40 progressive retinal degenerative 40 aldehyde dehydrogenase 40 cardiomyopathies 40 de ath 40 congenital deficiency 39 asperger syndrome 39 hay fever allergic rhinitis 39 Portrait Scenery Macro 39 genetic mutations 39 Tourette Syndrome TS 39 gallstones 39 BRCA2 gene mutations 39 hereditary nonpolyposis colon cancer 39 gallstone disease 39 aphthous stomatitis 39 definitively diagnose 39 Usher syndrome 39 urolithiasis 39 constipation predominant 39 genetic mutation 39 inherited genetic mutation 39 cortical cataract 39 congenital muscular dystrophies 39 Prenatal diagnosis 39 Goldenhar syndrome 39 muscle degeneration 39 genetic trait 39 H pylori 39 congenital disorders 39 biological predisposition 39 TCF#L# 39 skeletal malformations 39 fibrosing cardiomyopathy 39 IEA underestimates 39 mutations 39 justice Lossmann 39 BRCA1 gene 39 heritable genetic 39 neonatal respiratory distress 39 paternal lineage 39 Nicotine dependence 39 OCA2 39 exotropia 39 potentially modifiable 39 cirrhotic liver 39 congenital cataract 39 inheritable diseases 39 susceptibility alleles 39 adenomatous polyps 39 SLC#A# gene [001] 39 seborrhea 39 nutrient deficiency 39 Lewy body 39 captivity orcas 39 incurable degenerative brain 39 optic atrophy 39 dysmorphic 39 incomplete penetrance 39 chromosomal abnormalities 39 haemorrhagic 39 itching sneezing 39 Dr. Shawn Agharkar 39 immuno deficiency 39 colorectal polyps 39 Urinary tract infection 39 nephron 38 monogenic disorders 38 hereditary 38 inherited retinal 38 subfertility 38 genetic variant 38 Vitamins B6 38 atopy 38 Neurofibromatosis Type 38 long QT syndrome 38 component phosphatidylserine PS 38 valvular heart disease 38 polyps growths 38 spongiform encephalopathies 38 maternally transmitted 38 vitamin deficiencies 38 haplotype 38 blindness deafness 38 pigmentosa 38 sacral agenesis 38 cardiovascular cerebrovascular 38 hypotonia 38 obesity sedentary lifestyle 38 Nasal allergies 38 liver disease 38 hypoplasia 38 fructose intolerance 38 non syndromic 38 congenital abnormalities 38 inheritable 38 fatty liver disease 38 YouTube behaves Fricklas 38 Levys foundations 38 flashbulb memories 38 exfoliative glaucoma 38 spondylolysis 38 polycystic kidneys 38 predisposing factors 38 congenital abnormality 38 disease 38 malignancy 38 genetic predisposition 38 cystic fibrosis sickle cell 38 Arrivals halls 38 obstructive coronary artery 38 genetically predisposed 38 thrombophilia 38 liver cirrhosis 38 granulosa cell 38 diaphragmatic hernia 38 TP# mutations 37 diverticular disease 37 Treacher Collins 37 congenital scoliosis 37 #q# [001] 37 Autosomal dominant 37 fat soluble vitamin 37 lymphatic vasculature 37 fibrodysplasia ossificans progressiva 37 alleles 37 leaky gut 37 pareidolia 37 cervical spondylosis 37 EDNOS 37 VUR 37 adjective counterrevolutionary continue 37 Cetomimidae 37 aY chromosome 37 Hostage rescues 37 DICER1 37 Gerry McNellis 37 eosinophilic inflammation 37 Genetic susceptibility 37 GLENN GREENWALD 37 depot antipsychotics 37 malformations 37 damn fishing DiNero 37 immunodeficiency diseases 37 Hypertrophic Cardiomyopathy HCM 37 recessive genes 37 Syndrome SADS 37 Mr. NOCERA 37 congenital disorder 37 Perthes disease 37 dust mite allergies 37 chromosome #q# [002] 37 symbol GAM Pr 37 TMJ temporomandibular joint 37 cancerous enlargement 37 premorbid 37 Checkout PayPal 37 L methionine 37 mutant gene 37 dietary boogeymen 37 Moebius Syndrome 37 nonsteroidal anti inflammatories 37 metabolic disturbances 37 renal scarring 37 premalignant lesions 37 Polymorphic Ventricular Tachycardia CPVT 37 nitrofurantoins 37 Sturge Weber 37 chronically constipated 37 UGT#B# 36 choice Heeren Graber 36 canker sores 36 vitamin deficiency 36 PESTLE segment 36 NOAA Lehr 36 Fat soluble vitamins 36 cervical uterine 36 Attention Deficit Disorder ADD 36 PZ Tel 36 uncurable 36 steamroll Sharapova 36 Pdx1 36 anti convulsants 36 renal carcinoma 36 disorder thalassemia 36 CYP#E# 36 intriguing subplot fizzled 36 food intolerances 36 noncancerous 36 chromosomal aberration 36 metachromatic leukodystrophy 36 racemic mixture 36 binary opposites 36 benign breast 36 optic nerve hypoplasia 36 SRY gene 36 noisy bustling Rustaveli 36 thyroxin 36 aggression Lacinak 36 SAMe 36 dopamine transporter gene 36 rheumatic heart 36 Homeopathic medicines 36 causally linked 36 protein tyrosine phosphatases 36 ozone layer HFCs 36 recessive mutations 36 osteodystrophy 36 vitamin folic acid 36 unexplained infertility 36 dysplasia 36 bowel polyps 36 genetically homogeneous 36 childhood leukemia 35 osteogenesis imperfecta OI 35 ventricular dysplasia 35 agenesis 35 breast cancer Klatsky 35 IBS IBS 35 cirrhosis 35 inheritable genetic 35 genetic defects 35 amygdalin 35 Dissociative Identity Disorder 35 onset Alzheimer disease 35 peptic ulcer 35 Bovine spongiform encephalopathy BSE 35 prenatal ultrasounds 35 emm 35 fastbuild kit 35 Gordon Yoesting 35 drown Woolas 35 hereditary diseases 35 germinal centers 35 subluxations 35 periodontal infections 35 congenital deformity 35 buys bagged spinach 35 adaptogens 35 worse Nakamine 35 heredity 35 cryptorchidism 35 Arthrogryposis Multiplex 35 speak unpleasant truths 35 Worthingtons testified 35 Lacroix Saint Laurent 35 autism dyslexia 35 consanguineous marriages 35 Brain plasticity 35 MICHAEL BESCHLOSS 35 accusation Lumumba 35 singular verb 35 germline 35 SERGIO GARCÍA 35 KRULWICH 34 #p# [001] 34 contained PGM ounces 34 bureaucratic massaging 34 God Mizaal 34 monoamine oxidase inhibitors 34 cetirizine Zyrtec 34 HIV subtype 34 Lady Rai nursemaid 34 phenotype 34 retinitis pigmentosa degenerative 34 deafness 34 Nassau Bahamas Info 34 coincidence Trentadue 34 Europa 2C 34 vertebra slips 34 embed Lapan 34 predisposes 34 MAOIs 34 childhood leukaemias 34 armpit lymph nodes 34 Sophia Nakano 34 Mylo ilikemusic 34 profound deafness 34 cheetahs Bolt 34 atopic 34 inherited degenerative 34 Pop Tart Shripka 34 STACY LEWIS 34 triptans 34 BRCA2 mutation 34 glandular 34 cancerous polyps 34 lockout Gabbert 34 batteries Linhardt 34 questioner chimes 34 chromosome #q# [001] 34 pilots spatial disorientation