Sort   by:  
 Page size 
TranscriptomicsCpG Island methylation variation in placentae of Intra-Uterine Growth Restricted (IUGR) fetuses versus controls
Methylation profiling of CpG Island Methylation of genomic DNA samples extracted from placentae of Intra-Uterine Growth Restricted newborns and gestational age matched controls. These data can be used for methylation comparisons between these two types of samples. The results of such comparisons can...
ORGANISM(S): Homo sapiens 
2011-04-11 | E-GEOD-22326 | biostudies-arrayexpress
UnknownBent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.
Not available
S-EPMC3309195 | biostudies-literature
UnknownGATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder.
Not available
S-EPMC7920571 | biostudies-literature
UnknownData sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository.
Not available
S-EPMC8523590 | biostudies-literature
UnknownVariant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.
Not available
S-EPMC9473360 | biostudies-literature
UnknownHistone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients.
Not available
S-EPMC7821880 | biostudies-literature
Unknown<i>PIK3CA</i>-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution.
Not available
S-EPMC5019182 | biostudies-literature
UnknownBi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.
Not available
S-EPMC6408318 | biostudies-literature
Sort   by:  
 Page size