Genetic heterogeneity of congenital dyserythropoietic anemia type II

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Genetic heterogeneity of congenital dyserythropoietic anemia type II

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Aggressive systemic mastocytosis with the co-occurrence of PRKG2::PDGFRB, KAT6A::NCOA2, and RXRA::NOTCH1 fusion transcripts and a heterozygous RUNX1 frameshift mutation.

Concurrent chromothripsis events in a case of TP53 depleted acute myeloid leukemia with myelodysplasia-related changes.

CD55 is a HIF-2α marker with anti-adhesive and pro-invading properties in neuroblastoma.

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ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.

MicroRNA expression profiling in male and female familial breast cancer.

A new reporter strategy reveals a subset of nonmigratory hematopoietic stem cells located in a dynamic bone marrow niche.

A randomized phase 2 study combining midostaurin, low-dose cytarabine and venetoclax in newly diagnosed AML ≥60 years.

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DGAT1, but Not DGAT2, Is Required for Ovarian Lipid Storage and Egg Hatchability in Rhodnius prolixus.

The limits of genetic screening: trisomy 21 after euploid preimplantation genetic testing for aneuploidy and negative noninvasive prenatal testing.

Correlation of whole-body fat content and its distribution with lumbar fat content under different age, gender and BMI conditions: quantitative analysis of MRI based on deep learning.

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