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UnknownCorrelating Neuroimaging and CNVs Data: 7 Years of Cytogenomic Microarray Analysis on Patients Affected by Neurodevelopmental Disorders.
Not available
S-EPMC8608469 | biostudies-literature
UnknownMaternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients.
Not available
S-EPMC4203356 | biostudies-literature
UnknownLoss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38.
Not available
S-EPMC4824604 | biostudies-literature
UnknownA CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder.
Not available
S-EPMC4104741 | biostudies-literature
UnknownMicroRNAs in seminal plasma are able to discern infertile men at increased risk of developing testicular cancer.
Not available
S-EPMC11977642 | biostudies-literature
UnknownExtracellular RNAs from Whole Urine to Distinguish Prostate Cancer from Benign Prostatic Hyperplasia.
Not available
S-EPMC11432375 | biostudies-literature
UnknownNF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome.
Not available
S-EPMC1285166 | biostudies-literature
UnknownRenal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets
Not available
S-EPMC9698586 | biostudies-literature
UnknownClinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations.
Not available
S-EPMC5384833 | biostudies-literature
UnknownDeletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome.
Not available
S-EPMC4789813 | biostudies-literature
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