Related by context. All words. (Click for frequent words.) 65 ductus arteriosus 65 Spina bifida occurs 64 Spina bifida 62 Anencephaly 61 anencephaly 60 mesoderm 59 myelomeningocele 59 neural tube defect 59 gastrulation 59 yolk sac 59 epididymis 59 thyroid hormone deficiency 59 corpus luteum 59 hemoglobin molecule 58 holoprosencephaly 58 epiphysis 58 lymphatic vasculature 58 ectopic 58 atrial septum 58 lissencephaly 58 spermatic cord 58 fertilized egg splits 57 myelination 57 cohesin 57 Fallopian tube 57 hypoplasia 57 neural crest cells 57 neuronal migration 56 patent foramen ovale 56 malformation 56 filaggrin 56 craniosynostosis 56 embryogenesis 56 neuromuscular junction 56 ureters 56 lobules 56 parathyroid gland 56 beta globin 55 inguinal canal 55 Gestational diabetes 55 HGPS 55 Thyroid hormone 55 DISC1 55 elastic fibers 55 patent ductus arteriosus 55 oviduct 55 progressive degeneration 55 atresia 55 neural tube defects NTDs 55 Beckwith Wiedemann syndrome 55 outflow tract 55 SMN protein 55 dentate gyrus 55 microdeletion 55 motor neurones 55 glottis 55 amniotic cavity 55 atrial septal defect 55 neuroepithelial cells 54 granule cells 54 endometrial lining 54 tubules 54 nerve degeneration 54 motor neuron degeneration 54 premature ovarian 54 centrosome 54 somites 54 ventricular septum 54 zona pellucida 54 CFTR gene 54 foramen ovale 54 Vangl2 54 thrombus blood clot 54 uterine wall 54 epiphyseal 54 hindbrain 54 electrical conduction 54 neural crest 54 septal 54 Pre eclampsia 54 ADPKD patients 54 cerebellum 54 ectoderm 54 podocyte 54 genetic imprinting 54 tricuspid valve 54 Scar tissue 54 spermatogenesis 54 morphogenesis 54 egg follicles 54 fallopian tube 54 protein tau 54 conceptus 54 cypin 54 chromosomal defect 54 microvasculature 54 IRAK1 54 duodenum 54 proinsulin 54 podocytes 54 Wnt signaling 54 Sox# 53 angular gyrus 53 meiosis 53 clot thrombus 53 Ectopia Cordis 53 hydrops 53 Insulin resistance 53 Purkinje cells 53 CHD7 53 choroid plexus 53 lymphatic vessels 53 vas deferens 53 cilium 53 neurofibromas 53 neuroligins 53 myofibroblasts 53 fibrous connective tissue 53 CDH# 53 testis 53 endometrial cells 53 ventricular septal defect 53 dendritic spines 53 dysgenesis 53 undeveloped conjoined twin 53 IRS1 53 epididymal 53 embryo implants 53 progerin 53 tricuspid atresia 53 exocrine glands 53 uterine cavity 53 Neural tube defects 53 mutant protein 53 malformations 53 atherosclerotic lesion 53 FMR1 gene 53 MECP2 gene 53 Apert syndrome 53 GATA4 53 ventricular septal defects 53 primordial germ cells 53 pharyngeal 53 genetic defect 53 spindle fibers 53 catalytic subunit 53 trophoblast cells 53 bronchi 53 Eclampsia 53 skeletal malformations 53 transfusion syndrome 53 situs inversus 53 fibrotic tissue 53 nephrons 53 dystrophin protein 53 lymphoid tissue 53 autophagic 53 HMGA2 52 MECP2 52 MLL gene 52 primordia 52 neurone 52 caveolae 52 AV node 52 Preeclampsia 52 agenesis 52 ductus 52 β catenin 52 tubule 52 diaphragmatic hernia 52 venous drainage 52 patent foramen ovale PFO 52 glia cells 52 spinal column 52 molar pregnancy 52 Charcot foot 52 atrial tissue 52 Eustachian tube 52 clotting cascade 52 ectopia cordis 52 DISC1 gene 52 developmental abnormalities 52 diverticula 52 congenital abnormalities 52 membranous 52 collagen fibers 52 HOX genes 52 chick embryos 52 cerebral hemispheres 52 heterotaxy 52 spina bifida defect 52 placenta praevia 52 NR#A# 52 fetal membranes 52 myelin insulation 52 parathyroid glands 52 Endometrial cancer 52 germ cells 52 toxic amyloid beta 52 urethral sphincter 52 pre eclamptic 52 Sudden infant 52 ectodermal 52 chromatin structure 52 pulmonary hypoplasia 52 intra uterine 52 fusiform 52 Folate deficiency 52 excess uric acid 52 pelvic cavity 52 retinal dysfunction 52 proximal tubule 52 prematurity ROP 52 atrial septal defects 52 mitotic spindle 52 diaphyseal 52 skeletal deformities 52 myelin fatty substance 52 neural tube defects 52 misfolds 52 exocrine 52 adrenal cortex 52 Cyclin D1 52 ovary 52 teratoma 52 congenital anomalies 52 anencephaly fatal 52 amnion 52 placental 52 Aortic stenosis 52 congenital anomaly 52 umbilical hernias 52 fibrin deposition 52 periosteal 52 ureter 52 desmosomes 52 Sox9 52 epigenetic modification 52 blood vessels 52 Uric acid 52 cholestasis 52 acrosome reaction 52 ovarian follicle 51 brain malformation 51 esophageal atresia 51 DNA methylation patterns 51 pulmonary arteries 51 ventricle 51 LKB1 51 congenital abnormality 51 T cadherin 51 telomeres shorten 51 tumor suppressor gene 51 Sonic Hedgehog 51 bladder sphincter 51 uterus cervix 51 congenital disorder 51 myotonic dystrophy 51 Spinal stenosis 51 papilla 51 nephron 51 mesenchyme 51 organelle 51 melanocyte 51 Notch signaling 51 pyloric stenosis 51 thyroid hormone 51 SLC#A# gene [001] 51 Cleft lip 51 Dilated cardiomyopathy 51 chromosomal abnormality 51 folic acid deficiency 51 radial glia 51 Hutchinson Gilford progeria 51 LIS1 51 enteric nervous 51 phthalate syndrome 51 mesothelial cells 51 notochord 51 primordial follicles 51 RPE# 51 peritoneum 51 uterus womb 51 organogenesis 51 Six3 51 myocyte 51 microvessels 51 Cysts 51 Hypoplastic Left Heart 51 sirenomelia 51 endocrine glands 51 heart syndrome HLHS 51 Broca area 51 polyhydramnios 51 Pax6 51 trophoblasts 51 forebrain 51 ADAMTS# 51 cultured neurons 51 pulmonary venous 51 BMP signaling 51 amyloid deposits 51 KCNE2 51 desmin 51 subventricular zone 51 tunica vaginalis 51 Math1 51 autoregulation 51 TSLP 51 WAGR syndrome 51 systemic amyloidosis 51 proteoglycan 51 C1q 51 glomerular 51 nucleoli 51 fatty infiltration 51 secretes insulin 51 uterus 51 intraventricular 51 neuroligin 51 pineal 51 abnormal curvature 51 Hutchinson Gilford Progeria Syndrome 51 mouse embryos 51 Gestational age 51 functional dystrophin protein 51 gyrus 51 Rh incompatibility 51 bronchus 51 gastroschisis 51 amino acid metabolism 50 GATA3 50 NF1 50 incompetent cervix 50 Rb gene 50 lymphatics 50 ovule 50 epithelial tissues 50 calcium homeostasis 50 IRF6 50 glial cells 50 lymph vessels 50 eustachian tube 50 Hemangiomas 50 cysts 50 neurofibroma 50 umbilical vein 50 Obstetric fistula 50 hyperactivated 50 morphogen 50 tetramer 50 toxemia 50 nerve cells 50 luminal surface 50 fibrillin 1 50 articular surface 50 hypospadias 50 myometrium 50 centromere 50 colocalization 50 bicuspid valve 50 aneuploidy 50 blastocyst 50 cardiac hypertrophy 50 atrioventricular septal defect 50 recurrent laryngeal nerve 50 endometrial tissue 50 oligohydramnios 50 Pulmonary hypertension 50 arterioles 50 basal ganglia 50 directly degrades fibrin 50 thoracic aortic aneurysm 50 cerebellar 50 sister chromatids 50 tibial sesamoid 50 protein dystrophin 50 oocyte 50 hormone secretion 50 dorsolateral 50 tau protein 50 PKD1 50 normal prion protein 50 axon guidance 50 LPA receptors 50 CIB1 50 vertebrate embryos 50 atherosclerotic lesions 50 factor PlGF 50 necrotizing enterocolitis 50 hypoplastic 50 intracytoplasmic sperm injection 50 collagen VI 50 meningeal 50 frontotemporal 50 Amyloid beta 50 undifferentiated stem cells 50 n cofilin 50 spongy tissue 50 FGF signaling 50 biliary atresia 50 aortic valve stenosis 50 placenta accreta 50 Intussusception 50 senile plaques 50 X inactivation 50 atrioventricular 50 gestational sac 50 persistent pulmonary hypertension 50 Diabetic neuropathy 50 merozoites 50 retinal ganglion cell 50 amniotic membranes 50 growth restriction IUGR 50 mastoid 50 chromosomal anomalies 50 cerebro spinal fluid 50 photoreceptors 50 mesothelium 50 insulin secreting beta 50 epithelia 50 excitatory synapses 50 optic nerve 50 ADPKD 50 actin cytoskeleton 50 amyloid plaque 50 fetu 50 thyroid hormones 50 pulmonary stenosis 50 luteal cells 50 prevent neural tube 50 male hormone androgen 50 Purkinje cell 50 inherited mutations 50 efferent 50 DICER1 50 ERK2 50 bile ducts 50 p# mutations 50 BMP4 50 rhodopsin 50 vermis 50 nuchal 50 hemichannels 50 Nodules 50 obliterative bronchiolitis 50 neuro degenerative disease 50 embryological 50 cellular prion protein 50 leiomyomas 50 polycystic ovary syndrome 50 fatty plaques 50 VHL gene 50 Foetal 50 mutated protein 50 cone photoreceptors 50 skeletal muscle cells 50 pancreas 50 vomeronasal organ VNO 50 Adhesions 50 de novo mutations 50 sensory cortex 50 mitochondrial dysfunction 50 breast lobules 50 FMR1 50 histone protein 50 PTEN gene 50 epithelial cells lining 50 adherens junctions 50 proNGF 50 aneurysmal 50 cornea clouding vision 50 insulin signaling pathway 50 synaptic 50 hormones secreted 50 atherosclerotic plaques 50 beta globin gene 50 oocyte maturation 50 mucus glands 50 blastocyst stage 50 Avascular necrosis 50 Crouzon syndrome 50 MeCP2 gene 50 disulfide bond 50 Hypospadias 50 coarctation 50 cystine 49 subchondral bone 49 hamartoma 49 sinus node 49 placental abruption 49 abnormalities 49 resorbed 49 hyperactivation 49 Pten 49 metaphyseal 49 trophoblast 49 hyoid 49 neuronal synapses 49 Crouzon Syndrome 49 trophoblastic 49 interstitium 49 misfolding 49 klotho 49 physis 49 Holoprosencephaly 49 Ebstein anomaly 49 intrauterine infection 49 blastomeres 49 cerebellar vermis 49 inflamed tissues 49 ovulatory cycles 49 regulates gene expression 49 myogenesis 49 truncus arteriosus 49 congenital brain tumor 49 posterior fossa 49 Focal dystonia 49 epithelium 49 vasculature 49 distraction osteogenesis 49 dendritic spine 49 intracerebral 49 #BP# 49 metabolic derangements 49 DNA rearrangements 49 intestinal tissue 49 AMPA receptors 49 Iron deficiency anemia 49 synapse formation 49 ovules 49 amniotic fluid embolism 49 amyloid beta plaques 49 interferon pathway 49 ovarian follicles 49 toxic beta amyloid 49 lactase deficiency 49 humeral head 49 skeletal dysplasia 49 cystic 49 stroma 49 cardiac fibroblasts 49 mammary cells 49 preterm babies 49 Neural tube 49 genomic instability 49 seminiferous tubules 49 limb deformities 49 congenital disorders 49 phosphorylates 49 cerebral arteries 49 FoxO1 49 blastema 49 TGF ß 49 osteochondroma 49 malignant transformation 49 Dystrophin 49 amyloid beta plaque 49 trachea windpipe 49 arterial calcification 49 superior mesenteric artery 49 epigenetic changes 49 mitral stenosis 49 FXTAS 49 neurite 49 elastin fibers 49 telomere maintenance 49 collagen VII 49 aneuploidies 49 lateral ventricle 49 atrioventricular valve 49 Smad4 49 C EBP alpha 49 phrenic nerve 49 filaggrin gene 49 metaphase 49 cortical neurons 49 urate crystals 49 synaptogenesis 49 retinal pigment epithelium 49 Hypothyroidism 49 reproductive tract 49 neuromotor 49 chromosomal instability 49 HLHS 49 inferior vena cava 49 mammary tissue 49 Hox gene 49 TORC2 49 metabolic abnormality 49 subarachnoid space 49 glutamate receptors 49 TFIIH 49 thrombi 49 chromosomal abnormalities 49 calculi 49 onset sepsis 49 insulin secreting cells 49 caspase activation 49 MMP# 49 chondrocyte 49 fatty acid oxidation 49 Folic acid deficiency 49 perivascular 49 huntingtin 49 carpal bones 49 metabolize cholesterol 49 polyomavirus nephropathy 49 collagenase 49 Alu RNA 49 kisspeptin 49 Metastases 49 chorionic villi 49 periventricular 49 neural cells 49 PIP3 49 pericardium 49 polycystic kidneys 49 presenilin 49 dystrophin gene 49 microcracks 49 amyloid fibrils 49 membrane rupture 49 PrPC 49 cleavage furrow 49 neuronal cell 49 tumoral 49 periventricular leukomalacia 49 F actin 49 biochemical signaling pathway 49 opportunistic viral infection 49 neurites 49 Obstructive sleep apnea 49 chromosomal rearrangement 49 brainstem 49 extracellular matrix ECM 49 defects CHDs 49 Gastroparesis 49 neuronal circuits 49 zygotic 49 jejunum 49 vesicle 49 mesenteric 49 thyroid hormone levels 49 prolactin hormone 49 endometrium 49 Maternal obesity 49 glomerulus 49 Benign tumors 49 amyloid deposition 49 clefting 49 Prox1 49 erythrocytes 49 primary visual cortex 49 basal lamina 49 alveolar bone 49 placental function 49 neural fibers 49 aortic arch 49 facial clefts 49 pre eclampsia 49 CFTR protein 49 synovial membrane 49 nitric oxide synthase 49 Smad3 49 centrosomes 49 hereditary disorder 49 ovaries 49 normal prion proteins 49 non coding RNA 49 pancreatic endocrine 49 Chronic inflammation 49 NOTCH1 49 neuronal dysfunction 49 arteriovenous fistula 49 coiled coil 49 Cx# [001] 49 SCN5A 49 female reproductive tract 49 resorb 49 galactose 49 secretase 49 congenital malformations 49 huntingtin protein 49 chromosome #q#.# [001] 49 Hoxb8 49 chromosome abnormality 49 synovial cells 49 plexiform 49 p# pathway 49 septal defects 49 corpus callosum 48 cells cardiomyocytes 48 endoplasmic reticulum 48 Oxidative stress 48 vesicular 48 leptin signaling 48 neuroblastoma tumor 48 Mitochondrial 48 ductal 48 DiGeorge Syndrome 48 hypocretin neurons 48 thymus 48 pAkt 48 predisposing factor 48 tumor suppressor protein 48 Gestational diabetes occurs 48 bone deformities 48 ciliated 48 osteoblastic 48 INF2 48 neurotransmitter norepinephrine 48 abnormal chromosomes 48 hormone insulin 48 blood clot thrombus 48 NKX2 48 receptor molecule 48 molecular pathway 48 vacuole 48 fibular 48 Diabetic retinopathy 48 Klotho gene 48 atrial septal 48 alveoli 48 DLX5 48 subcutaneous tissues 48 female hormones estrogen 48 cerebral vasospasm 48 NF2 48 dystroglycan 48 Pleural mesothelioma 48 granulosa cell 48 plasminogen 48 PTEN protein 48 TEL AML1 48 neovascularization 48 pancreas gland 48 achromatopsia 48 Aβ 48 ventricles 48 protein fragment 48 autosomal dominant 48 fetal fibronectin 48 cervix 48 glandular tissue 48 aneuploidy screening 48 neuronal pathways 48 progesterone hormone 48 neuroblasts 48 preeclamptic women 48 granulosa cells 48 cardiac fibrosis 48 ruptured uterus 48 dentine 48 cholinergic neurons 48 NICHD sponsors research 48 polycystic 48 terminal ileum 48 CaM kinase II 48 Spinal muscular atrophy 48 PrP 48 adipocytes fat 48 cerebral ventricles 48 embryonic tissues 48 diverticulum 48 Jhdm2a 48 skeletal abnormalities 48 ciliary 48 Wnt pathway 48 SRY gene 48 pituitary hormone 48 mutant mouse 48 lymphatic tissue 48 Cholangiocarcinoma 48 intestinal epithelial cells 48 cilia 48 cartilaginous 48 dominantly inherited 48 enzyme lactase 48 cells secrete 48 CTCF 48 comedones 48 Bankart lesion 48 Dpp 48 leiomyoma 48 oxidized lipids 48 Hox genes 48 fetal malformations 48 pancreatic duct 48 marrow cavity 48 motoneurons 48 posterior vitreous detachment 48 calcineurin 48 neuronal degeneration 48 lamin 48 retinal nerve 48 Cdc# 48 hippocampal function 48 ferroportin 48 Hypertrophy 48 mosaicism 48 reproductive abnormalities 48 myelin sheath 48 insulates nerve fibers 48 osteopetrosis 48 acrosome 48 TP# gene 48 APOL1 48 fertilized embryo 48 milk ducts 48 trabecular bone 48 gastrointestinal GI tract 48 motor neuron 48 lysosomes 48 DiGeorge syndrome 48 primary cilia 48 terminally differentiated 48 septal defect 48 erectile tissue 48 folate deficiency 48 vascular dysfunction 48 fibrous tissue 48 proto oncogene 48 preterm infants 48 senescent cells 48 Ovulation 48 Hemolytic Uremic Syndrome HUS 48 secretory cells 48 aortic wall 48 myometrial 48 CRTAP 48 spinous processes 48 hamartomas 48 piRNAs 48 involution 48 synaptic function 48 patent ductus arteriosus PDA 48 p# mutation 48 XBP1 48 ileum 48 pharynx 48 Kufs disease 48 untreated celiac disease 48 hypothalamic 48 cochlear nerve 48 uterine lining 48 gluconeogenesis 48 ovaries fallopian tubes 48 antioxidant enzyme 48 cervical dilation 48 Sensorineural hearing loss 48 foramen magnum 48 #q#.# [002] 48 fibrillin 48 cell nuclei 48 synovium 48 Fibroid tumors 48 causative genes 48 vascular endothelial cells 48 galactosemia 48 Wynshaw Boris 48 lamellar 48 renal calculi 48 infertility miscarriages 48 dysplastic 48 Methylmercury 48 Methyl mercury 48 chromosomal disorder 48 leptin receptor 48 dysplasias 48 transmit electrical impulses 48 pelvic girdle 48 periosteum 48 Osr2 48 Genetic mutation 48 dermoid cyst 48 ventricular remodeling 48 baroreceptors 48 KATP channels 48 sized gland 48 sinoatrial node 48 endocrine tumors 48 neuroendocrine 48 hyperparathyroidism 48 IGF2 48 intestinal lining 48 MCAD deficiency 48 chromosomes 48 retinal vein 48 suppresses tumor 48 genetic abnormality 48 microtubule dynamics 48 hepatic vein 48 Transverse myelitis 48 tonsillar 48 HbF 48 Ago2 48 osteoblast 48 da mage 48 chromosomal translocation 48 oncomodulin 48 fibrin clots 48 myomas 48 disfigurations birthmarks 48 gamma globin gene 48 ectopic pregnancy 48 vascular occlusion 48 osseointegration 48 seminal vesicle 48 vitreous gel 48 p# gene 48 hedgehog signaling 48 mammary gland 48 Dr. Loeken 48 fibroblast cells 48 digestive organs 48 catenin 48 autocrine 48 amyloid proteins 48 secretory pathway 48 neonatal respiratory distress 48 pyelonephritis 48 muscle degeneration 48 anovulation 48 lateral curvature 48 bone deformity 48 MCADD 48 maturational 48 chorioamnionitis 48 aneurysm sac 48 dyskeratosis congenita 48 cystic fibrosis transmembrane conductance 48 mammalian embryo 48 endoplasmic reticulum ER 48 grafted stem cells 48 ductal breast cancer 48 Sleep apnea occurs 48 epigenetic alterations 48 NMDA receptors 48 cerebri 48 acetyl CoA 48 stromal 48 POMC neurons 48 SHANK3 48 XBP 1 48 dynamin 47 adult neurogenesis 47 homologous chromosomes 47 junctional 47 Hirschsprung disease 47 arteriotomy site 47 excitotoxicity 47 spinal canal 47 pulmonary valve 47 male reproductive tract 47 hormone aldosterone 47 neonate 47 hippocampal neurons 47 Ectopic pregnancies 47 neurodevelopmental disorder 47 presynaptic 47 microtia 47 MLL2 47 acetabulum 47 oligodendrocytes 47 protein beta amyloid 47 acinar 47 congenital cataract 47 benign polyps 47 Cryptococcus neoformans 47 biliary 47 Fragile X mental retardation 47 Smad7 47 birth defect 47 echogenic 47 Lafora disease 47 cadherin 47 acetylcholine neurotransmitter 47 antral follicles 47 Neural stem cells 47 mammalian embryos 47 vaginal childbirth 47 GSTT1 47 kidney tubules 47 Vitamin B9 47 LRAT 47 demyelination 47 Retinopathy 47 locus coeruleus 47 neural tissues 47 fibrogenesis 47 mTORC1 47 diseased valves 47 encodes protein 47 dopaminergic cells 47 spectrin 47 hydronephrosis 47 marsupial mammals 47 chromosome