developmental abnormalities

Related by string. * DEVELOPMENTAL . Developmental : Mental Health Developmental Disabilities . developmental disability . developmental delays . developmental psychologist . Developmental Disabilities shelved / Abnormalities : additional cytogenetic abnormalities . fetal abnormalities . rhythm abnormalities . chromosome abnormalities . physiological abnormalities * *

Related by context. All words. (Click for frequent words.) 72 reproductive abnormalities 72 congenital disorders 70 malformations 70 inherited mutations 70 genital abnormalities 69 chromosomal anomalies 69 neurological abnormalities 69 abnormalities 69 phthalate syndrome 69 de novo mutations 69 congenital anomalies 68 aneuploidies 68 congenital malformations 68 neuropsychiatric disorder 68 congenital abnormalities 67 recurrent miscarriages 67 skeletal deformities 67 myopathies 67 Folic acid deficiency 66 Genetic mutations 66 polyhydramnios 66 brain lesions 66 bone deformities 66 utero exposure 66 epigenetic changes 66 undescended testicles 66 epigenetic modification 65 IUGR 65 neurodevelopmental disorder 65 dominantly inherited 65 thyroid dysfunction 65 chromosome rearrangements 65 biochemical abnormalities 65 neuronal dysfunction 65 Hip dysplasia 65 chromosomal disorders 65 hydrops 65 persistent pulmonary hypertension 65 prenatal exposures 65 behavioral abnormalities 65 G6PD deficiency 65 deafness neurological 65 pAkt 65 holoprosencephaly 64 CHD7 64 limb deformities 64 Iron deficiency anemia 64 motor neuron degeneration 64 genetic syndromes 64 facial clefts 64 metabolic abnormalities 64 epigenetic alterations 64 monogenic 64 mental retardation epilepsy 64 chromosomal anomaly 64 enterocolitis 64 genetic abnormalities 64 limb malformations 64 neurological sequelae 64 ovarian dysfunction 64 shortened telomeres 64 hamartomas 64 bone marrow mesenchymal stem 64 thyroid hormone levels 64 chromosomal abnormalities 64 neuro developmental disorders 64 testicular tumors 64 mitochondrial dysfunction 64 fetal malformations 64 anatomical abnormalities 64 Genetic variants 64 microdeletion 63 Leydig cell 63 monozygotic twins 63 mitochondrial mutations 63 chorioamnionitis 63 mtDNA mutations 63 predisposing factor 63 neurofibromas 63 dysgenesis 63 transfusion syndrome 63 heterotaxy 63 neuro developmental 63 severe dehydrating diarrhea 63 hypoplasia 63 hyperinsulinemia 63 Hemangiomas 63 phthalate exposure 63 leptin deficiency 63 gastric carcinoma 63 neurodevelopmental 63 neurosensory 63 hemolytic disease 63 chromosome abnormalities 63 chromosomal rearrangement 63 hormonal abnormalities 63 NPHP 63 Beckwith Wiedemann syndrome 63 hereditary predisposition 63 neurological degeneration 63 dysplasias 62 genetic defects 62 highly heritable 62 thyroid hormone deficiency 62 neural tube defect 62 recessive genetic 62 ovarian hormones 62 Cysts 62 postnatally 62 MCAD deficiency 62 primary ciliary dyskinesia 62 retinal dysfunction 62 physiological abnormalities 62 hyperinsulinism 62 folic acid deficiency 62 dysmorphic features 62 DNA methylation patterns 62 hydatid disease 62 neurologic complications 62 germline mutations 62 chromosomal defect 62 autosomal dominant disorder 62 Hashimoto thyroiditis 62 Birth defects 62 Genetic predisposition 62 cystic fibrosis chronic pancreatitis 62 Magnesium deficiency 62 Mycoplasma pneumoniae 62 anovulation 62 Wernicke Korsakoff syndrome 62 Apert syndrome 62 leiomyomas 62 hyperstimulation 62 nerve degeneration 62 Neural tube defects 62 phenotypic variation 62 pyloric stenosis 62 chromosomal alterations 62 deformities 62 da mage 62 periventricular leukomalacia 62 hereditary deafness 62 myelomeningocele 62 clefting 61 prenatally diagnosed 61 HGPS 61 neuritic 61 neurodevelopment 61 uterine tumors 61 neuroligins 61 mucus glands 61 Prion diseases 61 etiologic 61 cause cardiac channelopathies 61 intraventricular hemorrhage 61 Abnormalities 61 alexithymia 61 retinal vascular 61 cystic fibrosis muscular dystrophy 61 bronchopulmonary dysplasia 61 #q#.# [002] 61 Rh incompatibility 61 #q#.# deletion syndrome 61 congenital defects 61 chromosome abnormality 61 neurodevelopment disorder 61 cholestasis 61 Malignant tumors 61 infertility miscarriages 61 recurrent miscarriage 61 untreated celiac disease 61 endocrine abnormalities 61 coma convulsions 61 hyperactivation 61 mitochondrial defects 61 deafness meningitis 61 Folate deficiency 61 congenital blindness 61 gastrointestinal dysfunction 61 mitochondrial DNA mutations 61 metabolic dysfunction 61 undiagnosed celiac disease 61 neuroinflammation 61 hamartoma 61 placenta praevia 61 enterovirus infection 61 homozygosity 61 Fibroid tumors 61 dizygotic twins 61 IgA deficiency 61 paraneoplastic 61 congenital adrenal hyperplasia CAH 61 male reproductive tract 61 Viral infections 61 Stress hormones 61 androgen excess 61 hyperplastic 61 chromosomal aberrations 61 genetically inherited 61 Hair follicles 61 seizures comas 61 Hutchinson Gilford progeria 61 polycystic ovarian syndrome PCOS 61 chromosomal instability 61 AAT deficiency 61 genetic imprinting 61 atopic diseases 61 lactase deficiency 61 Kufs disease 61 osteosarcomas 61 mammary gland tumors 61 preterm deliveries 61 ADPKD 61 metabolic abnormality 61 intermittent hypoxia 61 precocious puberty 61 muscular dystrophy cystic fibrosis 61 Mitochondrial diseases 61 chromosomal disorder 61 Gliomas 61 autosomal recessive 61 autoinflammatory diseases 61 lung lesions 61 Autoimmune disorders 61 hyperammonemia 61 hypothalamic pituitary 61 Hyperthyroidism 61 extramedullary 61 craniofacial anomalies 61 methylation patterns 61 medium chain acyl 61 NF1 61 neonatal encephalopathy 61 airway hyperresponsiveness 61 Meckel Gruber 61 teratogens 61 intracerebral 61 neurodevelopmental disorders 61 breast endometrial 60 idiopathic generalized epilepsy 60 Iron deficiency 60 subfertility 60 ectodermal dysplasia 60 congenital birth defects 60 hypercalcaemia 60 HbF 60 malformation 60 nonvascular 60 hyperprolactinemia 60 hematological abnormalities 60 immunodeficiencies 60 Arrhythmogenic Right Ventricular Cardiomyopathy 60 sexually dimorphic 60 Spinal muscular atrophy 60 Genetic mutation 60 oral clefts 60 astrocytomas 60 microvascular disease 60 familial ALS 60 neurodevelopmental outcomes 60 Chlamydia pneumoniae 60 KCNH2 60 pleiotropic effects 60 prostate abnormalities 60 Cryptococcus neoformans 60 gene MECP2 60 neurocognitive deficits 60 adrenal cortex 60 pancreatic endocrine 60 polycystic ovary syndrome PCOS 60 structural abnormalities 60 pituitary tumors 60 umbilical hernias 60 CHDs 60 parkinsonism 60 perinatal asphyxia 60 immunodeficiency 60 epithelial tissues 60 Vitamin B# deficiency 60 stress hormone corticosterone 60 bacteriuria 60 genital defects 60 Leptospira 60 Dilated cardiomyopathy 60 folate metabolism 60 meningitis encephalitis 60 LIS1 60 antiphospholipid syndrome 60 Zinc deficiency 60 Dwarfism 60 autistic traits 60 congenital hypothyroidism 60 Trichophyton rubrum 60 congenital anomaly 60 reproductive toxicity 60 bacteria Streptococcus pneumoniae 60 prematurity ROP 60 normal karyotype 60 Ribavirin causes 60 hypogonadotropic hypogonadism 60 neuroendocrine 60 inbreeding depression 60 congenital CMV 60 PTPN# 60 dysregulation 60 degenerative neurological diseases 60 diaphragmatic hernia 60 coagulopathy 60 muscle degeneration 60 cryptorchidism 60 hormone imbalances 60 interstitial fibrosis 60 endocrine disruption 60 FMRP protein 60 Bacterial vaginosis 60 cirrhosis liver failure 60 Heavy menstrual bleeding 60 hippocampal function 60 Intussusception 60 masculinization 60 Pulmonary hypertension 60 progressive neurodegenerative disorder 60 ultrastructural 60 behavioral disinhibition 60 infertility miscarriage 60 de ath 60 skeletal abnormalities 60 genital deformities 60 neuromotor 60 hydrocephaly 60 bronchopulmonary dysplasia BPD 60 karyotypes 60 microdeletions 60 JAK mutations 60 atherosclerotic lesions 60 Angelman syndrome 60 metabolic disturbances 60 Selenium deficiency 60 Sjögren syndrome 60 neurodevelopmental outcome 60 chromosome #q#.# [001] 60 ambiguous genitalia 59 Malassezia 59 neuropsychological impairments 59 Klinefelter syndrome 59 Ehrlichia 59 neuroblastomas 59 amyloid deposition 59 hormonal disturbances 59 LRRK2 mutations 59 Bardet Biedl syndrome 59 congenital cataract 59 environmental toxicants 59 embryonic tissues 59 penile fibrosis 59 GBA mutations 59 malignant transformation 59 chromosomal defects 59 polymorphic ventricular tachycardia 59 reproductive endocrine 59 Genetic variations 59 penetrance 59 ichthyosis vulgaris 59 nonhereditary 59 guinea pigs lubiprostone 59 ataxias 59 spongiform encephalopathies 59 thyroid tumors 59 myeloproliferative neoplasms 59 cerebellar 59 monozygotic 59 leaky gut 59 untreated hypothyroidism 59 Li Fraumeni syndrome 59 genital malformations 59 impair fertility 59 autosomal dominant polycystic kidney 59 mutant huntingtin protein 59 p# activation 59 selenium deficiency 59 autosomal recessive disease 59 paralytic illness 59 penile cancers 59 missense mutations 59 periodontal tissues 59 #q#.# [001] 59 metabolic acidosis 59 multisystem disorder 59 SMAD4 59 Prenatal exposure 59 Hypertrophic 59 chorionic villi 59 blindness deafness 59 immunodeficiency disorder 59 neuro degenerative disease 59 cognitive deficits 59 Leydig cells 59 endocrine disrupting 59 monozygotic twin 59 brain neurochemistry 59 Diabetic neuropathy 59 neurological impairment 59 tumoral 59 mosaicism 59 Skeletal muscle 59 Osteogenesis imperfecta 59 genetic loci 59 Tuberous sclerosis 59 airway irritation 59 craniofacial deformities 59 mammary tumors 59 biochemical imbalances 59 phenotypic differences 59 chromosomal rearrangements 59 polycystic ovary syndrome 59 endocrine tumors 59 Beta thalassemia 59 differential gene expression 59 exotropia 59 Hurler syndrome 59 Hirschsprung disease 59 synaptic function 59 Thyroid hormone 59 Radiographic findings 59 atopic disorders 59 GH deficiency 59 involuntary tics 59 FASPS 59 fatal myelination disorder 59 ependymomas 59 irregular menstrual periods 59 genetic polymorphism 59 vascular dysfunction 59 molar pregnancy 59 fronto temporal dementia 59 autonomic dysfunction 59 cretinism 59 hypoperfusion 59 fibrotic disease 59 tissue necrosis 59 inherited genetic mutations 59 #q# deletion 59 LVNC 59 alpha synuclein protein 59 hemorrhagic colitis 59 leiomyoma 59 neuro developmental disorder 59 cardiac malformations 59 mesotheliomas 59 Genetic variation 59 monoclonal gammopathy 59 familial pancreatic cancer 59 otitis 59 Ovarian cysts 59 thyrotropin levels 59 orofacial clefts 59 maternally inherited 59 congenital deafness 59 subclinical 59 von Hippel Lindau 59 infarcts 59 spontaneous mutation 59 channelopathies 59 mitochondrial diseases 59 pathophysiological 59 epigenetic silencing 59 hypocalcaemia 59 Cushing syndrome 59 epigenetic markers 59 chromosomal abnormality 59 Atopic eczema 59 trophoblast cells 59 Meckel Gruber syndrome 59 pathophysiologic 59 neonatal morbidity 59 sexual dimorphism 59 GPC5 59 SHANK3 59 Secondhand smoke exposure 59 embryonal 59 bone marrow suppression 59 chromosomal deletions 59 Male infertility 59 hyperparathyroidism 59 neonatal respiratory distress 59 FXTAS 59 ANCA associated 59 orchitis 59 spinocerebellar ataxia 59 inherit predisposition 59 spontaneous mutations 59 alveolar epithelial cells 59 neuropsychological deficits 59 inherited predisposition 59 behavioral disturbances 59 autosomal recessive disorder 58 urolithiasis 58 unknown etiology 58 EoE 58 neuropsychiatric diseases 58 Digoxin toxicity 58 lymph node enlargement 58 allergic dermatitis 58 Vitamin D insufficiency 58 azoospermia 58 preeclamptic 58 alpha thalassemia 58 testicular germ cell 58 gastric distention 58 intracytoplasmic 58 fibroma 58 systemic amyloidosis 58 PrPC 58 MECP2 gene 58 Acidosis 58 neurofibrillary 58 polycystic kidneys 58 underactive thyroid gland 58 radiographic findings 58 anemia thrombocytopenia 58 estrogenic effects 58 fetal chromosomal 58 Chromosomal abnormalities 58 herpesviruses 58 necrotizing 58 allergic sensitization 58 thyrotropin 58 spontaneous miscarriages 58 osteochondrosis 58 neurological disorder affecting 58 physiological characteristics 58 CNTNAP2 58 folate deficiency 58 sCJD 58 estrogen deficiency 58 Systemic lupus 58 growth restriction IUGR 58 Childhood Disorder 58 Becker muscular dystrophy 58 STAT4 58 p# mutations 58 syndrome FAS 58 hypercoagulability 58 egg follicles 58 VUR 58 cecal 58 hyper IgE syndrome 58 Nutritional deficiencies 58 bacteraemia 58 eccrine 58 asthma rhinitis 58 medulloblastomas 58 Leber hereditary optic neuropathy 58 sporadic Creutzfeldt Jakob 58 Retinopathy 58 demodex 58 endocrine glands 58 biochemical imbalance 58 aortic atherosclerosis 58 abnormal genital 58 convulsions coma 58 Periodontal disease 58 PTEN mutations 58 abnormal chromosomes 58 BCL#A 58 pituitary hormone 58 hypoxic ischemic brain 58 tricuspid atresia 58 MYCN amplification 58 precancerous cervical 58 methicillin susceptible Staphylococcus aureus 58 Menkes disease 58 motor neurones 58 deafness blindness 58 nephrogenic 58 homocystinuria 58 reproductive hormones 58 inherited retinal degeneration 58 chlamydial infections 58 lung cancer asbestosis 58 neurological dysfunction 58 activated microglia 58 alkalosis 58 gastric ulceration 58 birth defects 58 previously undescribed 58 lymphatic vasculature 58 thyroid abnormalities 58 Premature Ovarian Failure 58 neural tube defects NTDs 58 intrauterine infection 58 phenotypic variability 58 subclinical hypothyroidism 58 pulmonary hypoplasia 58 polyglutamine diseases 58 Postnatal depression 58 maternally derived 58 calcium deficiency 58 Aortic aneurysms 58 lipomas 58 skeletal dysplasia 58 phthalate metabolites 58 elevated cortisol 58 developmental disorders 58 dopaminergic cells 58 PCOD 58 abnormal vaginal bleeding 58 galactosemia 58 severe congenital neutropenia 58 idiopathic pulmonary 58 #p#.# [001] 58 intestinal epithelium 58 familial adenomatous polyposis 58 testicular dysgenesis syndrome 58 phonic tics 58 Abscesses 58 genetic abnormality 58 reproductive disorders 58 Tay Sachs thalassemia 58 Maternal obesity 58 necrotising 58 cystic ovaries 58 genus Plasmodium 58 excitotoxic 58 WDR# 58 craniofacial defects 58 dysautonomia 58 neurologic deficits 58 Hypertrophic cardiomyopathy 58 Hereditary angioedema 58 SCA1 58 neuron degeneration 58 Toxoplasmosis 58 Fatty liver 58 Pancreatic insufficiency 58 born preterm 58 varicoceles 58 optic atrophy 58 undescended testes 58 ectoderm 58 chronic autoimmune disorder 58 pyelonephritis 58 Cloned animals 58 untreated sleep apnea 58 neurologic symptoms 58 commonest cause 58 excitotoxicity 58 nonsense mutation 58 progressive degeneration 58 CYP#B# 58 heterozygotes 58 Morquio syndrome 58 spontaneous abortions 58 Malformations 58 Nanobacteria 58 Oxidative stress 58 fibroids endometriosis 58 chromosomal imbalance 58 maturational 58 obesity insulin resistance 58 tumorigenicity 58 APOE ε4 58 cerebellar vermis 58 gastroenteritis conjunctivitis 58 Elevated serum 58 WAGR syndrome 58 intestinal microflora 58 RSV infections 58 chromosomal translocations 58 p# mutation 58 ABCB1 58 sonographic diagnosis 57 predisposing factors 57 T1DM 57 nongenetic 57 nutritional deficiency 57 Male pattern baldness 57 microglial 57 germline cells 57 Wernicke encephalopathy 57 dermatophytes 57 familial clustering 57 coinfection 57 lysosomal diseases 57 prematurely abort 57 pathogenetic mechanisms 57 Eisenmenger syndrome 57 sarcoids 57 congenital abnormality 57 parkinsonian 57 Ebstein anomaly 57 neurologic disorders 57 BMPR2 57 epigenetic modifications 57 myometrium 57 Metastases 57 neuro degenerative disorders 57 genetic polymorphisms 57 mesothelial cells 57 Idiopathic 57 neurodegenerative disorder 57 bullous pemphigoid 57 Demodex 57 penile erection 57 Infant botulism 57 AAT Deficiency 57 genotoxic stress 57 genetic mutations Spoor 57 Colon polyps 57 thoracic aortic aneurysm 57 Aeromonas 57 papillomas 57 gene deletions 57 placental insufficiency 57 dysmotility 57 trophoblastic 57 recessive trait 57 spinal muscle atrophy 57 hypothalamic pituitary adrenal axis 57 aneuploidy 57 retinitis pigmentosa RP 57 carotid atherosclerosis 57 genetic susceptibility 57 FGFs 57 amino acid metabolism 57 Equine piroplasmosis 57 Neurological disorders 57 Periodontitis 57 Invasive fungal infections 57 phenotypic expression 57 mitochondrial disorders 57 inherited neurological disorder 57 Chronic inflammation 57 lichen planus 57 C. pneumoniae 57 genetic determinants 57 genetic mutations 57 lymphangiogenesis 57 demyelinating disease 57 Streptococcus pneumoniae Haemophilus influenzae 57 R. equi 57 haematopoietic 57 neural crest stem cells 57 tetany 57 pituitary adenoma 57 endocannabinoid signaling 57 Peutz Jeghers syndrome 57 spontaneously aborted 57 fat malabsorption 57 hypercalciuria 57 antiphospholipid antibodies 57 Hereditary angioedema HAE 57 genetic alterations 57 arterial calcification 57 nodular lesions 57 microvessels 57 axonal degeneration 57 Fungal infections 57 unprovoked seizures 57 endocasts 57 A. fumigatus 57 thyrotoxicosis 57 LPA receptors 57 causative mutation 57 hormones secreted 57 microbiomes 57 Neural stem cells 57 prenatal exposure 57 coagulation abnormalities 57 congenital disorder 57 SIADH 57 androgen depletion 57 blindness paralysis 57 periventricular 57 Bacterial infections 57 Methylmercury 57 leukoencephalopathy 57 Joubert syndrome 57 thyroiditis 57 gestational diabetes mellitus GDM 57 periodontal diseases 57 Helicobacter infection 57 sporadic ALS 57 prepubertal 57 necrotizing enterocolitis 57 cardiac fibrosis 57 menstrual abnormalities 57 multisystem disease 57 lymphomas leukemias 57 mental retardation cerebral palsy 57 renal scarring 57 varicella infection 57 secrete hormones 57 cytomegalovirus infection 57 hypotonia 57 ectopic expression 57 hay fever asthma 57 hypoxic ischemic encephalopathy 57 ductal breast cancer 57 toxicosis 57 hormonal disorder 57 NAGS deficiency 57 hereditary disorders 57 Neurofibromatosis type 57 EBV infection 57 TCF#L# gene 57 PON1 57 calculi 57 infantile hemangioma 57 MeCP2 gene 57 congenital adrenal hyperplasia 57 hirsutism 57 filaggrin 57 atresia 57 Leukemias 57 degenerative disorders 57 neuropsychiatric disorders 57 amyloid peptide 57 prostate carcinogenesis 57 gene rearrangements 57 MC4R gene 57 epilepsies 57 olfactory dysfunction 57 hypopituitarism 57 meningiomas 57 NOMID 57 PBDE exposure 57 CTVT 57 NAFLD 57 genetic defect 57 Trichomonas 57 Chlamydia psittaci 57 Androgenetic alopecia 57 protozoan parasites 57 tryptase 57 mental retardation blindness 57 Neural tube 57 frontotemporal 57 hormonal stimulation 57 genomic imprinting 57 Fas ligand 57 recessively inherited 57 enamel defects 57 moderately heritable 57 Polymorphic Ventricular Tachycardia CPVT 57 Crouzon Syndrome 57 pulmonary metastasis 57 dysregulated 57 sonographic appearance 57 endotoxemia 57 colorectal carcinogenesis 57 fusiform 57 discoid lupus 57 ovarian hyperstimulation syndrome 57 autoimmune thyroid 57 placental tissues 57 upper airway obstruction 57 LRP5 57 antibody IgE 57 cardiac dysfunction 57 aetiological 57 pheochromocytoma 57 cAMP signaling 57 Chronic pancreatitis 57 perinatal complications 57 FMR1 57 hydronephrosis 57 Cleft lip 57 congenital malformation 57 Pelvic Inflammatory Disease 57 ERK signaling 57 encephalitis inflammation 57 Epileptic seizures 57 ectopic 57 superior mesenteric artery 57 nulliparous 57 cerebral ischemia 57 Skin rashes 57 hematopoietic cancers 57 respiratory gastrointestinal 57 vitamin B1 deficiency 57 Cystic fibrosis CF 57 IGF1 57 neuronal migration 57 Sensorineural hearing loss 57 somatic mutation 57 gastrointestinal GI perforation 57 MYH9 57 postoperative delirium 57 genital tract infections 57 obstructive coronary artery 57 asplenia 57 Brugada syndrome 57 protein tau 57 pathogenetic 57 PDGFR 57 primary hyperparathyroidism 57 underlying pathophysiology 57 gait disturbance 57 herpes simplex encephalitis 57 podocytes 57 amyloid beta plaques 57 congenital deformities 57 Polycystic ovary syndrome PCOS 57 prion infections 57 brachial plexus palsy 57 hepatic renal 57 diabetic microvascular complications 57 fungus Fusarium 57 organochlorines 57 hypermethylated 57 viral etiology 57 epididymitis 57 #ß HSD1 57 immunocompromised individuals 57 sickle cell cystic fibrosis 57 Glucocorticoids 57 ductal adenocarcinoma 57 multifactorial disease 57 hyperactivated 57 Sporadic CJD 57 cervical lymph nodes 57 flaccid paralysis 57 CP CPPS 57 PGD PGS 57 pathophysiological mechanisms 57 Atopic dermatitis 57 motor neuron diseases 57 acetabular dysplasia 57 INF2 57 malarial anemia 57 myocardial fibrosis 57 nonsense mutations 57 kidney urologic 57 transgene expression 57 hereditary hemochromatosis 57 Bronchiolitis 57 neurotoxic effects 57 fibrous dysplasia 57 atherothrombosis 57 unmeasured factors 57 megacolon 57 polydactyly 57 autosomal dominant inheritance 57 maternally transmitted 57 dyskeratosis congenita 57 nephropathy kidney 57 leukaemias 57 overactivation 57 Dental fluorosis 57 bicuspid aortic valves 57 histopathological 57 auditory neuropathy 57 seminomas 56 neurological complications 56 Yeast infections 56 hypoxia ischemia 56 MCADD 56 vulval 56 rhinovirus infection 56 Preterm babies 56 Diabetic nephropathy 56 paralysis blindness 56 CDH1 56 Hh pathway 56 secondary bacterial infections 56 striatal neurons 56 tremors numbness 56 deformed limbs 56 hypertrophic cardiomyopathy HCM 56 #p#.# [002] 56 fatal neurodegenerative 56 myocardial dysfunction 56 Severe Primary IGFD 56 chronic hepatitis cirrhosis 56 miRNA expression 56 allelic variation 56 Oxidative damage 56 atrophic gastritis 56 encephalitis meningitis 56 chitinase 56 hypokalemia hypomagnesemia 56 hormonal imbalances 56 TSC1 56 Entamoeba histolytica 56 nonalcoholic steatohepatitis 56 included exfoliative dermatitis 56 serotonin defects 56 Colorectal cancers 56 Myocardial infarction 56 liver scarring 56 dizygotic 56 Congenital 56 tunica vaginalis 56 hepatocellular 56 Obstetric fistula 56 colic diarrhea 56 irreversible blindness 56 Premature birth

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