The dataset consists of records from whole exome sequecing and bioinformatic analysis which includes genes and gene variants from a Mexican family with recurrence for gastroschisis (two affected half-sisters with gastroschisis, mother, and father of the proband). Release of this dataset was based on the Human Genome annotation, GRCh37/hg19.
Published in Data
Gastroschisis is one of the most prevalent human birth defects concerning the ventral body wall development. Recent research has given a better understanding of gastroschisis pathogenesis through the identification of multiple novel pathogenetic pathways implicated in ventral body wall closure. Deciphering the underlying genetic factors segregating...
Dataset of Pedigree, genotypes, clinical and biochemical characteristics of families of Northeastern Mexico