chromosome abnormalities

Related by string. * Chromosome . Chromosomes . chromosomes : Y chromosome . chromosome #q# [001] . chromosome #q# [002] . inactive X chromosome . aY chromosome . chromosome aberrations / Abnormalities : additional cytogenetic abnormalities . fetal abnormalities . rhythm abnormalities . physiological abnormalities . chromosomal abnormalities . congenital abnormalities * *

Related by context. Frequent words. (Click for all words.) 72 chromosomal abnormalities 68 genetic abnormalities 67 aneuploidy 65 congenital anomalies 62 abnormalities 61 neural tube defect 59 congenital abnormalities 59 genetic defects 59 mitochondrial dysfunction 59 congenital malformations 59 genetic abnormality 58 mutations 58 trisomy 58 genetic defect 57 fetal abnormalities 57 chromosomal abnormality 56 LQTS 56 CNVs 56 gene mutations 56 CMV infection 56 BRCA1 gene 56 mitochondrial diseases 56 NF1 55 neurodevelopmental disorders 55 malformations 55 hereditary breast cancer 55 metabolic abnormalities 55 gene mutation 55 imprinted genes 55 Fanconi anemia 55 genetic mutations 54 mutation 54 DNA methylation 54 prenatal diagnosis 54 genetic alterations 54 genetic variant 54 beta thalassemia 54 neurodevelopmental 54 gene variants 54 chromosomal 54 polycystic ovary syndrome 54 cytogenetic 53 BRCA2 mutations 53 mammary tumors 53 gene expression patterns 53 ectopic pregnancies 53 ovarian function 53 ASDs 53 genetic mutation 53 mutated gene 53 ovarian tumors 53 heterozygous 53 premature menopause 53 ectopic 53 anencephaly 53 defective gene 53 mutated genes 53 neoplasm 53 behavioral abnormalities 53 male infertility 52 adenoma 52 methylation 52 Hakonarson 52 poorer prognosis 52 overdiagnosis 52 mtDNA 52 situ hybridization 52 pre cancerous lesions 52 genetic disorders 52 thyroid cancers 52 Trisomy 52 miRNAs 52 genetic alteration 52 neurological complications 52 susceptibility gene 52 NAFLD 52 susceptibility genes 51 gene expression profiles 51 single nucleotide polymorphism 51 neoplasms 51 alleles 51 spontaneous abortions 51 immunodeficiency 51 primary biliary cirrhosis 51 prenatally 51 glycosylation 51 homozygous 51 germ cells 51 thyroid function 51 genetic variants 51 Rett syndrome 51 febrile seizures 51 non coding RNAs 51 structural abnormalities 51 tumor suppressor gene 51 prion disease 51 medulloblastoma 51 bladder cancers 51 BRCA mutations 51 histologic 50 BRCA2

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