Related by context. All words. (Click for frequent words.) 71 Premature ovarian 67 unexplained infertility 66 premature menopause 65 polycystic ovary syndrome 65 primary ovarian insufficiency 63 subfertility 63 preserved ejection fraction 62 polycystic ovary syndrome PCOS 62 irregular menstrual cycles 62 polycystic ovarian syndrome PCOS 62 recurrent miscarriages 61 ovulate 61 fibroids endometriosis 61 anovulation 61 familial adenomatous polyposis 60 placenta praevia 60 thyroid dysfunction 60 leiomyomas 60 undergoing hysterectomy 60 polycystic ovarian syndrome 60 Polycystic Ovary Syndrome 60 ovulatory cycles 60 chromosomal abnormalities 60 infertility miscarriage 60 thrombophilia 60 Heavy menstrual bleeding 60 subclinical hypothyroidism 60 hypopituitarism 59 bronchopulmonary dysplasia BPD 59 skeletal malformations 59 atypical hyperplasia 59 recurrent miscarriage 59 ductal breast cancer 59 anovulatory 59 hypothalamic amenorrhea 59 familial hypercholesterolemia 59 Hashimoto thyroiditis 59 PCOD 59 aneuploidy 59 basal cell nevus syndrome 58 holoprosencephaly 58 dominantly inherited 58 de novo mutations 58 FXTAS 58 inherited mutations 58 cryptorchidism 58 mosaicism 58 chorioamnionitis 58 blocked fallopian tubes 58 congenital abnormalities 58 hyperemesis 58 underlying pathophysiology 58 hypogonadotropic hypogonadism 58 gestational hypertension 58 overt hypothyroidism 58 monozygotic twin 58 Vitamin D insufficiency 58 T1DM 58 Fragile X gene 58 penetrance 58 oophorectomy 58 aneuploidies 58 testicular tumors 57 galactosemia 57 invasive carcinoma 57 dyskeratosis congenita 57 nonischemic 57 neural tube defect 57 pituitary hormone 57 aneuploid 57 precancerous cervical 57 autosomal recessive 57 ovarian 57 placenta accreta 57 nonhereditary 57 Endometrial cancer 57 hormone FSH 57 subfertile 57 microdeletion 57 Pulmonary hypertension 57 aortic valve stenosis 57 BRCA1 mutations 57 chromosomal disorders 57 amenorrhoea 57 ovulation induction 57 G6PD deficiency 57 mammary cancers 57 microvascular disease 57 primary biliary cirrhosis 57 IgA deficiency 57 Hypothyroidism 57 Gestational diabetes 57 BRCA2 breast cancer 57 trophoblastic 57 egg follicles 57 Premature Ovarian Failure 57 intraventricular hemorrhage 57 abnormal uterine bleeding 57 pathophysiologic 57 infertility 57 estrogen deficiency 57 transfusion syndrome 57 chromosomal anomalies 57 AUDs 57 testicular germ cell 57 menstrual irregularity 57 untreated celiac disease 57 Testosterone deficiency 57 ovarian stimulation 57 metabolize cholesterol 57 Apert syndrome 57 Beckwith Wiedemann syndrome 57 bacteriuria 56 genetic abnormalities 56 adenomyosis 56 molar pregnancy 56 Klinefelter syndrome 56 NF1 56 endometrial hyperplasia 56 Polycystic ovary syndrome 56 underactive thyroid gland 56 Prostate enlargement 56 genes predisposing 56 pattern baldness 56 prenatally diagnosed 56 hereditary hemochromatosis 56 neurocognitive deficits 56 postnatally 56 ovarian dysfunction 56 Ovarian cysts 56 myocardial fibrosis 56 lactase deficiency 56 congenital anomalies 56 ADPKD 56 multiple gestations 56 hamartomas 56 mutated BRCA1 56 insulin secreting beta 56 anovulatory infertility 56 phthalate syndrome 56 chromosomal defect 56 gastric carcinoma 56 BRCA2 carriers 56 Anencephaly 56 aneuploidy screening 56 uterus didelphys 56 diagnosed prenatally 56 uterine tumors 56 pre eclamptic 56 Von Willebrand disease 56 vitro maturation 56 chromosome abnormality 56 neurofibromas 56 persistent pulmonary hypertension 56 fetal malformations 56 GH deficiency 56 leptin deficiency 56 familial ALS 56 ovarian function 56 FMR1 gene 56 Vitamin B# deficiency 56 corpus luteum 56 lobular breast cancer 56 induce ovulation 56 Folate deficiency 56 autoimmune thyroiditis 56 urolithiasis 56 intracerebral 56 Mitochondrial diseases 56 azoospermia 56 IVF ICSI 56 singleton pregnancy 56 Polycystic Ovarian Syndrome PCOS 56 Androgenetic alopecia 56 MYCN amplification 56 liver cirrhosis liver 56 poorer prognosis 55 Genetic predisposition 55 polycystic ovaries 55 atypia 55 diabetes mellitus DM 55 ovarian hyperstimulation 55 ELBW infants 55 hamartoma 55 neurofibrillary 55 monozygotic twins 55 hydrops 55 Aortic stenosis 55 antiphospholipid syndrome 55 Rh incompatibility 55 polycystic ovarian disease 55 pyloric stenosis 55 subclinical 55 karyotypes 55 MGUS 55 embryonal 55 homozygous FH 55 fetal chromosomal 55 abnormal chromosomes 55 thyroiditis 55 thyrotropin levels 55 postoperative delirium 55 deletion 5q 55 dizygotic twins 55 digest lactose 55 ovarian hyperstimulation syndrome OHSS 55 HbF 55 androgen deprivation 55 polycystic 55 euthyroid 55 KRAS oncogene 55 adrenal function 55 normal karyotype 55 congenital disorders 55 autologous transplants 55 Neurofibromatosis type 55 BRCA mutation 55 leukaemias 55 undescended testes 55 peripartum cardiomyopathy 55 cystic fibrosis chronic pancreatitis 55 inherited predisposition 55 genetic syndromes 55 untreated chlamydia 55 cardiac insufficiency 55 perimenopausal women 55 HGPS 55 left ventricular systolic 55 relapsed ALL 55 germline mutations 55 pituitary tumors 55 IPAH 55 LPA receptors 55 Severe Primary IGFD 55 hypercoagulability 55 amenorrhea 55 monogenic 55 bicuspid valve 55 metabolic disturbances 55 BRCA gene mutations 55 ectopic 55 myelomeningocele 55 Kufs disease 55 neuro degenerative disease 55 Hurler syndrome 55 postmenopausal estrogen 55 epididymitis 55 retrograde ejaculation 55 Myocardial infarction 55 Peutz Jeghers syndrome 55 ovarian follicles 55 CYP#D# gene 55 nonsense mutation 55 Polycystic Ovary Syndrome PCOS 55 BRCA mutations 55 MYH9 gene 55 HNPCC 55 diastolic heart 55 abnormal pap smears 54 autosomal recessive genetic 54 dysfunctional voiding 54 ovarian hormones 54 hormonal stimulation 54 reproductive endocrine 54 RhD negative 54 ovulatory 54 pyelonephritis 54 thyroid deficiency 54 Urinary tract 54 varicocele 54 epigenetic changes 54 neural tube 54 polycystic ovary 54 GISTs 54 Hypogonadism 54 abnormal genital 54 beta adrenergic receptor 54 androgenic alopecia 54 endometrial cancers 54 cryptogenic stroke 54 premutation 54 congential 54 idiopathic generalized epilepsy 54 myomas 54 hemochromatosis 54 causative gene 54 renal allograft 54 BRIP1 54 Leydig cell 54 BRCA2 mutation 54 gestational diabetes mellitus 54 adnexal mass 54 IUGR 54 APOE ε4 54 hereditary predisposition 54 incidentalomas 54 mitochondrial dysfunction 54 hematopoietic cell 54 p# mutations 54 genetic imprinting 54 abnormal vaginal bleeding 54 intra uterine 54 severe congenital neutropenia 54 recessive trait 54 orchitis 54 intrauterine infection 54 FMR1 54 LRAT 54 progressive neurodegenerative disorder 54 CMV infection 54 folic acid deficiency 54 recurrent ovarian 54 psychiatric comorbidity 54 puerperal psychosis 54 GSTT1 54 #q#.# deletion syndrome 54 gallstone disease 54 Arrhythmogenic Right Ventricular Cardiomyopathy 54 premalignant 54 polyhydramnios 54 insulin resistance syndrome 54 gonadal 54 slow metabolizers 54 seminomas 54 arterial thickening 54 de ath 54 liver metastasis 54 autonomic dysfunction 54 cardiac hypertrophy 54 thyrotropin 54 Carcinoid tumors 54 autosomal dominant disorder 54 varicoceles 54 kidney allograft 54 menstrual abnormalities 54 autosomal dominant 54 autosomal recessive disease 54 p# mutation 54 PPCM 54 autosomal recessive disorder 54 neuropsychological impairments 54 APOE e4 54 Pelvic Inflammatory Disease 54 lymphomas leukemias 54 breast endometrial 54 intracytoplasmic sperm injection 54 Li Fraumeni syndrome 54 carcinoid tumor 54 MTHFR 54 developmental abnormalities 54 Premature ejaculation 54 BRCA1 mutation carriers 54 Urinary incontinence 54 nulliparous 54 congenital abnormality 54 filaggrin 54 Hirschsprung disease 54 neonatal respiratory distress 54 familial pancreatic cancer 54 Brugada syndrome 54 recessively inherited 54 overactive thyroid gland 54 BARD1 54 Fistulas 54 androgen deficiency 54 thyroid hormone deficiency 54 TNF blocker therapy 54 BRCA2 gene 54 diagnostic biomarker 54 familial hypercholesterolaemia FH 54 advanced adenoma 54 deafness neurological 54 Hemangiomas 54 impair fertility 54 CFTR gene 54 thoracic aortic aneurysm 54 nonischemic cardiomyopathy 53 renal scarring 53 lichen planus 53 Metastases 53 congenital deficiency 53 conceive naturally 53 Menkes disease 53 spinocerebellar ataxia 53 retransplantation 53 nonalcoholic steatohepatitis 53 fertilized egg splits 53 phenotypic expression 53 TP# mutation 53 hormonal abnormalities 53 Uterine cancer 53 chromosomal rearrangement 53 Meckel Gruber 53 pernicious anemia 53 ovarian hyperstimulation syndrome 53 Bacterial vaginosis 53 microchimerism 53 affective psychoses 53 parous women 53 CHD7 53 acute aortic dissection 53 teratoma 53 proliferative retinopathy 53 p# activation 53 leukemia AML 53 Alport syndrome 53 Iron deficiency anemia 53 Intussusception 53 MLH1 53 proximal colon 53 subclinical hyperthyroidism 53 NF2 53 elevated CRP 53 vascular dysfunction 53 MetS 53 systolic hypertension 53 oocyte retrieval 53 systemic amyloidosis 53 ambiguous genitalia 53 endometrial carcinoma 53 LVNC 53 MSH2 53 cardiac tamponade 53 hyperandrogenism 53 Hip fracture 53 ectodermal dysplasia 53 coinfection 53 primary ciliary dyskinesia 53 LHRH receptor positive 53 toxemia 53 autosomal dominant polycystic kidney 53 cystectomy 53 Aplastic anemia 53 hippocampal atrophy 53 AAT deficiency 53 congenital diaphragmatic hernia 53 MCAD deficiency 53 Lafora disease 53 bilateral oophorectomy 53 monoclonal gammopathy 53 hirsutism 53 dopaminergic cells 53 atrophic gastritis 53 irregular menstruation 53 BRCA1 mutation 53 vulvodynia 53 histological subtype 53 beta thalassemia 53 syngeneic 53 heavy menstrual bleeding 53 valvular 53 nonproliferative 53 heterozygotes 53 p#INK#a 53 irregular menstrual periods 53 BRCA gene mutation 53 phenylketonuria 53 Zinc deficiency 53 Lactose intolerance 53 histologic subtype 53 difficulty conceiving 53 diabetes insipidus 53 comorbid disorders 53 Malignant tumors 53 urethral stricture 53 adrenal exhaustion 53 mitochondrial mutations 53 spontaneous miscarriages 53 myeloproliferative neoplasms 53 heterotaxy 53 associated tremor ataxia 53 hypertension congestive heart 53 neurofibromatosis type 53 PTPN# 53 albumin excretion 53 overactive bladder symptoms 53 Endometrial 53 oesophageal adenocarcinoma 53 nerve degeneration 53 recurrent UTI 53 Severe Combined Immunodeficiency 53 exotropia 53 naturally occurring estrogen 53 osteopetrosis 53 Fecal incontinence 53 fibroma 53 microsatellite instability 53 primordial germ cells 53 thalassemia sickle cell 53 hydrocephaly 53 Mitral valve 53 MELAS syndrome 53 prematurity ROP 53 post transplant lymphoproliferative 53 Ebstein anomaly 53 secondary amenorrhea 53 BCL#A 53 Cowden syndrome 53 Hurthle cell 53 pulmonary hypoplasia 53 undergone hysterectomy 53 bronchopulmonary dysplasia 53 ARVD 53 wound dehiscence 53 neurogenic bladder 53 infertility miscarriages 53 cardiac fibrosis 53 activate p# 53 precancerous condition 53 gene MECP2 53 endocrine abnormalities 53 hermaphroditism 53 hypogonadal 53 systolic dysfunction 53 chronic granulomatous disease 53 familial clustering 53 hypoplasia 53 acinar cells 53 recurrent VTE 53 lobular cancer 53 lymphangioleiomyomatosis LAM 53 ovulations 53 type 1diabetes 53 Rh factor 53 onset diabetes mellitus 53 progressive dyspnea 53 Prostatitis 53 reproductive abnormalities 53 #q# deletion 53 dysgenesis 53 TCF#L# gene 53 hypercoagulable 53 neuropsychiatric disorder 53 CYP#C# gene 53 LHRH agonists 53 Hurler Syndrome 53 hypokalemia hypomagnesemia 53 kidney insufficiency 53 Venous thromboembolism 53 Retinopathy 53 BRCA2 gene mutation 53 luteal 53 SIADH 53 retinal degeneration 53 choriocarcinoma 53 placental malaria 53 bladder exstrophy 53 chromosomal disorder 53 multifactorial disease 53 symptomatic fibroids 53 multivariate adjustment 52 decompensated cirrhosis 52 egg retrieval 52 infantile hemangiomas 52 prostate carcinoma 52 untreated sleep apnea 52 postpartum hemorrhage 52 genetic polymorphism 52 telomeres shorten 52 autoimmune thyroid 52 uterine rupture 52 prostate cancer CaP 52 primary aldosteronism 52 BMPR2 52 Wernicke encephalopathy 52 1 diabetes T1D 52 PCNSL 52 Spinal muscular atrophy 52 Polycystic ovarian syndrome 52 fibrous dysplasia 52 involution 52 MELAS 52 myelogenous leukemia 52 nephrosis 52 GBA mutations 52 hyperplasia 52 Lupus nephritis 52 Eclampsia 52 mitochondrial metabolism 52 urethral strictures 52 abnormal methylation 52 acrosome reaction 52 hippocampal dysfunction 52 chromosomal anomaly 52 cryptogenic 52 atrioventricular valve 52 abnormal Pap smear 52 thyrotoxicosis 52 myelodysplasia 52 hormone aldosterone 52 sudden sensorineural hearing 52 testosterone deficiency 52 neurodevelopmental outcomes 52 adenomatous polyps 52 nonmelanoma skin cancers 52 hypoplastic 52 monozygotic 52 recessive genetic 52 Subclinical 52 preeclamptic 52 epilepsies 52 precocious puberty 52 hormonal disorder 52 neuritic 52 islet transplants 52 cystic lesions 52 renal transplants 52 Heterozygous 52 CHEK2 gene 52 Polycystic ovary syndrome PCOS 52 left ventricular dysfunction 52 growth restriction IUGR 52 multiorgan 52 hematologic disorders 52 mIU L 52 perimenopausal 52 Premature menopause 52 aortic stiffness 52 pancreatic adenocarcinoma 52 Gestational 52 bicuspid aortic valves 52 hyperinsulinemia 52 white matter hyperintensities 52 Dysplasia 52 invasive ductal 52 lysosomal storage diseases 52 myoma 52 apolipoprotein E gene 52 androgenetic alopecia 52 chromosomal defects 52 hematopoietic cancers 52 haemochromatosis 52 intractable epilepsy 52 von Hippel Lindau 52 squamous cell lung cancer 52 syndrome FXTAS 52 asymptomatic PAD 52 obstetric complications 52 metabolic abnormalities 52 intestinal polyps 52 haematopoietic 52 Cognitive impairment 52 skeletal dysplasia 52 IM progesterone 52 induced cardiomyopathy 52 chronic hepatitis cirrhosis 52 colorectal carcinoma 52 preserved systolic 52 neurologic sequelae 52 immunodeficiencies 52 Brugada Syndrome 52 chromosomal alterations 52 Male infertility 52 thyroid hormone levels 52 pulmonary stenosis 52 advanced neoplasia 52 sFlt 1 52 generalized epilepsy 52 granulosa cell 52 lysosomal storage disease 52 genes BRCA1 52 ectopic pregnancies 52 genetic makeups 52 Primary IGFD 52 carotid plaques 52 biopsied embryos 52 elevated triglyceride levels 52 Fanconi anemia 52 nodal metastases 52 abnormal Pap test 52 lobules 52 lobular carcinoma 52 narcolepsy cataplexy 52 hormone therapy estrogen 52 olfactory dysfunction 52 arrhythmogenic right 52 #q#.# [002] 52 thyroid nodules 52 benign gynecological 52 oocytes 52 intrahepatic 52 dilated cardiomyopathy DCM 52 painful menstrual periods 52 cause cardiac channelopathies 52 atypical ductal hyperplasia 52 RET PTC rearrangements 52 MeCP2 gene 52 spontaneously aborted 52 Thyroid nodules 52 metastatic lung cancer 52 hyperprolactinemia 52 secondary hyperparathyroidism 52 paraganglioma 52 cirrhotic 52 PALB2 52 carcinoid tumors 52 Androgen 52 Colon polyps 52 Postnatal depression 52 progranulin mutations 52 hepatectomy 52 hypothyroidism 52 Tuberous sclerosis 52 mtDNA mutations 52 pulmonary hypertension PH 52 amniotic fluid embolism 52 familial aggregation 52 pelvic prolapse 52 hyper IgE syndrome 52 thyroid carcinoma 52 fat malabsorption 52 fluid overload 52 uterus womb 52 MTHFR gene 52 placental abruption 52 rheumatoid arthritis lupus 52 Magnesium deficiency 52 situs inversus 52 medium chain acyl 52 allelic variants 52 hereditary nonpolyposis colorectal cancer 52 myopathies 52 urinary leakage 52 ventricular dysplasia 52 LIS1 52 undergo radical prostatectomy 52 Adjuvant chemotherapy 52 menorrhagia 52 chronic renal insufficiency 52 bone deformities 52 MCADD 52 Ectopic pregnancies 52 precancerous tumors 52 muscular dystrophy cystic fibrosis 52 PON1 52 menopause andropause 52 gestational diabetes mellitus GDM 52 Niemann Pick disease 52 MODY 52 testicular cancers 52 Li Fraumeni 52 bronchogenic carcinoma 52 antiphospholipid antibodies 52 chronic prostatitis 52 allogenic 52 intracytoplasmic sperm injection ICSI 52 asplenia 52 renal kidney 52 cervical carcinoma 52 Dravet syndrome 52 shorter telomere length 52 behavioral disinhibition 52 carotid stenosis 52 contralateral breast 52 menarche 52 uterine prolapse 52 serum estradiol 52 asymptomatic bacteriuria 52 nephrogenic 52 oligohydramnios 52 chromosomal instability 52 immunosuppressed 52 IVF cycles 52 benign polyps 52 hormonal disorders 52 parkinsonism 52 TACI mutations 52 folate deficiency 52 BRCA2 mutations 52 neonatal encephalopathy 52 CHEK2 52 motor neuron degeneration 52 POAG 52 familial polyposis 52 Sezary syndrome 52 PTEN gene 52 cholestasis 52 Preterm babies 52 neurological abnormalities 52 congenital adrenal hyperplasia CAH 52 E selectin 52 male reproductive tract 52 Autoimmune disorders 52 Male pattern baldness 52 mesangial 52 Cholangiocarcinoma 52 hippocampal function 52 irregular menses 52 pretransplant 52 Fibroid tumors 51 Anorexia nervosa 51 undergoing IVF 51 microdeletions 51 sCJD 51 tuberous sclerosis complex 51 luteal phase 51 CHD mortality 51 V Leiden 51 Compulsive hoarding 51 DNA methylation patterns 51 neurologic deficits 51 HLA identical 51 myotonic dystrophy 51 MC1R 51 operable breast cancer 51 unexplained mental retardation 51 recurrent wheezing 51 perimenopause 51 valvular heart disease 51 Clusterin 51 cerebral infarction 51 fructose intolerance 51 thyroid disorders 51 sexual dimorphism 51 Gynecomastia 51 periventricular leukomalacia 51 immunologically matched 51 mitochondrial disorders 51 colorectal adenoma 51 breast cancer genes BRCA1 51 colorectal neoplasia 51 nondiabetic 51 breast carcinoma 51 HIV HCV coinfected 51 pituitary adenoma 51 ejection fractions 51 transplanted kidneys 51 hyperparathyroidism 51 digest gluten 51 lupus rheumatoid arthritis 51 glomerulosclerosis 51 Urge incontinence 51 elevated cortisol 51 adenomatous 51 pancreatic endocrine 51 CYP# [002] 51 polycystic kidneys 51 pulmonary dysfunction 51 LV dysfunction 51 Chronic fatigue 51 progressive neurologic 51 genetic polymorphisms 51 Sandhoff disease 51 proliferative diabetic retinopathy 51 neurodevelopmental impairment 51 corneal graft 51 colorectal neoplasms 51 sporadic ALS 51 medulloblastoma tumors 51 pelvic inflammatory disease 51 FTLD 51 OSAHS 51 nulliparous women 51 gastric cardia 51 acute myocarditis 51 immunodeficiency 51 chromosomally normal 51 urethritis 51 testosterone supplementation 51 Candidiasis 51 BRCA1 BRCA2 51 HNSCC 51 gastro oesophageal reflux 51 polymorphic ventricular tachycardia 51 Becker muscular dystrophy 51 aortic rupture 51 endometrial 51 endometrial thickness 51 variceal bleeding 51 underactive thyroid 51 Androgenetic Alopecia 51 Hutchinson Gilford progeria 51 compensatory mechanisms 51 fusiform 51 Liver transplantation 51 genetically predetermined 51 adenoma 51 primordial follicles 51 Hereditary angioedema HAE 51 neurologic complications 51 spontaneous mutation 51 nonmelanoma skin cancer 51 ovariectomy 51 intracranial atherosclerosis 51 thyroidectomy 51 Rb gene 51 born preterm 51 neurocognitive impairment 51 Barrett esophagus BE 51 menstruate 51 abnormal glucose tolerance 51 JAK mutations 51 ovaries 51 chlamydial infection 51 ascites 51 androgenic hormones 51 gestational glucose intolerance 51 Wilms tumors 51 Hutchinson Gilford Progeria 51 distant metastases 51 congenital scoliosis 51 euthymic patients 51 incurable genetic 51 idiopathic 51 atresia 51 enterocolitis 51 hepatocellular 51 ovary 51 uterine scar 51 HLA matched 51 APOL1 51 MECP2 gene 51 spermatogenesis 51 Testicular cancer 51 menstrual irregularities 51 gastric varices 51 supratentorial 51 Diabetic neuropathy 51 Ovary removal 51 hyperplastic 51 hormonal deficiencies 51 abnormal pap smear 51 aplasia 51 congenital CMV 51 Nicotine dependence 51 β cell 51 Subarachnoid hemorrhage 51 Inflammatory bowel diseases 51 TSC1 51 nephropathy 51 sexually dimorphic 51 Dilated cardiomyopathy 51 hemolytic anemia 51 otosclerosis 51 metaplasia 51 anti Mullerian hormone 51 neoplasias 51 Sexual dysfunction 51 Apc 51 uncontrolled epilepsy 51 progranulin 51 TTTS 51 Uterine fibroids 51 cytomegalovirus infection 51 seminoma 51 Obstetric fistula 51 Chronic pancreatitis 51 ectopia cordis 51 renal transplantation 51 bulimia nervosa 51 prostate carcinogenesis 51 predisposing factors 51 osteosarcomas 51 lung fibrosis 51 predisposing factor 51 gonadotropins 51 #q# deletion syndrome 51 placental function 51 essential thrombocythemia 51 neonate 51 juvenile myelomonocytic leukemia 51 tricuspid atresia 51 hypothalamus pituitary 51 chronic idiopathic 51 HBeAg negative 51 neuroligins 51 Myocarditis 51 chemoresistant 51 chromosomally 51 molecular abnormalities 51 IDDM 51 epithelial ovarian 51 cirrhosis liver failure 51 Noonan Syndrome 51 Aortic dissection 51 Treg cell 51 heritable variation 51 vitamin D insufficiency 51 Sertoli cells 51 mucinous 51 VCFS 51 CDH1 51 adrenal suppression 51 Papillary 51 von Willebrand disease 51 inappropriate antidiuretic hormone SIADH 51 thromboembolic disease 51 clinically insignificant 51 ovarian malignancy 51 Frontal lobe 51 blood clotting disorder 51 lymphocyte activation 51 pathogenic mutations 51 trophoblasts 51 serous ovarian cancer 51 benign prostatic hypertrophy 51 genital lesions 51 adverse perinatal 51 sex hormones estrogen