Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes

Clinical and whole exome sequencing findings in children from Yunnan Yi minority ethnic group with retinitis pigmentosa: Two case reports

6 p | 2 | 2

Characterization of genetic aberrations in a single case of metastatic thymic adenocarcinoma

12 p | 11 | 1

Comprehensive genomic profiling aids in understanding the lesion origins of a patient with six synchronous invasive lung adenocarcinomas: A case study

6 p | 13 | 1

Prenatal findings in a fetus with X-linked recessive type of chondrodysplasia punctata (CDPX1): A case report with novel mutation

6 p | 11 | 0

TP53 and PTEN mutations were shared in concurrent germ cell tumor and acute megakaryoblastic leukemia

8 p | 7 | 0