Chromosomal analysis and short-term outcome of prenatally diagnosed complex congenital heart disease
The evolution and maintenance of trioecy with cytoplasmic male sterility
16p13.3 homologous sequences underlie microdeletions encompassing TBC1D24 and ATP6V0C
GATA1 insufficiencies in dysmegakaryopoiesis of myelodysplastic syndromes
Genomic Balancing Act: Deciphering DNA rearrangements in the Complex Chromosomal Aberration involving 5p15.2, 2q31.1 and 18q21.32
A Cohort Study of Individuals with Neurodevelopmental Disorders and/or Congenital Anomalies Investigated by High- Resolution Chromosomal Microarrays in Southern Brazil: The Significance of Autism Spectrum Disorder
Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformations: experience from a tertiary referral center
Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting
Meiotic recombination dynamics in plants with repeat-based holocentromeres shed light on the primary drivers of crossover patterning
From asexuality to sexual reproduction: a cyclical switch of gametogenic pathways in hybrids depends on ploidy level