Associated Papers
PROKR2 mutations and SPRY4 variants with uncertain significance in a Kallmann syndrome family: Incomplete penetrance.
Yuan Y et al.
Global Medical Genetics, 2025
A heterozygous SPRY4 variant identified in female infertility characterized by reduced oocyte potential and early embryonic arrest.
Xia L et al.
Human Reproduction (oxford, England), 2024
Clinicopathological and genetic characterization of radiotherapy-induced undifferentiated pleomorphic sarcoma following breast cancer: a case series of three tumors and comprehensive literature review.
Lei T et al.
Diagnostic Pathology, 2024
Select a paper to view details