chromosome deletion

Related by string. * Chromosomes . Chromosome . chromosomes : chromosome abnormalities . inactive X chromosome . chromosome #q# [001] . chromosome #q# [002] . aY chromosome . Y chromosome . chromosome aberrations / Deletion . Deletions . deletions : deletion defect delay . deletion 5q cytogenetic abnormality . insertions deletions . insertion deletion . #q# deletion . accidental deletion * *

Related by context. Frequent words. (Click for all words.) 61 #p# [001] 61 autosomal dominant 60 neurodevelopmental disorder 60 #q# [001] 59 Angelman syndrome 59 congenital disorders 58 CNVs 58 ependymoma 57 chromosomal disorder 57 Wilms tumor 57 hyperinsulinemia 56 susceptibility gene 56 genetic abnormality 56 NF1 56 Spina bifida 56 anencephaly 56 developmental abnormalities 56 achondroplasia 55 teratoma 55 Heredity 55 susceptibility genes 55 neurodevelopmental disorders 55 myositis 55 Chromosome 55 beta thalassemia 54 mitochondrial dysfunction 54 microRNA expression 54 Tay Sachs disease 54 chromosome abnormalities 54 aneuploidy 54 multifactorial 54 NF2 54 chromosomal abnormality 54 neoplasm 54 heritable 54 congenital anomalies 54 PANDAS 53 DISC1 53 karyotype 53 Oxidative stress 53 de ath 53 familial hypercholesterolemia 53 microcephaly 53 Glioma 53 Binge eating 53 genetically inherited 52 syndromes 52 breast carcinoma 52 polycystic ovary syndrome 52 prepubertal 52 hirsutism 52 Progeria 52 receptor gene 52 sensorineural hearing loss 52 thyroid dysfunction 52 Fanconi anemia 52 neuroendocrine 52 adenocarcinomas 52 lung adenocarcinoma 52 pheochromocytoma 52 aetiology 52 Retinoblastoma 52 genomic instability 52 sirenomelia 52 Insulin resistance 52 fatal neurodegenerative 52 precocious puberty 52 astrocytoma 52 APOE4 52 IGF1 52 biliary atresia 52 Fragile X Syndrome 52 neural tube defect 52 unknown etiology 52 Muscular dystrophy 52 Prader Willi syndrome 52 FSGS 51 ectopic 51 rhabdomyosarcoma 51 medulloblastoma 51 demyelination 51 cerebellar 51 primary biliary cirrhosis 51 recessive gene 51 Notch signaling 51 #q# [002] 51 mitochondrial diseases 51 hyperparathyroidism 51 systemic lupus erythematosus SLE 51 neurodegenerative disorder 51 mutated gene 51 carcinoid 51 trisomy 51 ApoE4 51 Hemophilia B 51 Cushing syndrome 51 Friedreich ataxia 51 Gestational diabetes 51 compulsive hoarding 51 chromosome 51 paroxysmal nocturnal hemoglobinuria

Back to home page