Aarya Mishra ’24 has worked in the research lab of Professor Christina Tzagarakis-Foster since fall 2022. Mishra works with DAX1, a nuclear hormone receptor. “In the cancer that I’m investigating now, ...

15q11–q13 paternal deletion NA Prader–Willi syndrome (patients typically followed by endocrinology) 176270 15q11–q13 maternal deletion NA Angelman syndrome (patients not normally followed by ...

Aggregation and modification of LDLs (low-density lipoproteins) promote their retention and accumulation in the arteries. This is a critical initiating factor during atherosclerosis. Macrophage ...

AIM: To present phenotypic variability of WT1-related disorders. METHODS: Description of clinical and genetic features of five 46,XY patients with WT1 anomalies. RESULTS: Patient 1: newborn with ...

Purpose: 46,XX testicular/ovotesticular differences/disorders of sexual development (TDSD/OTDSD) are rare in childhood and exhibit marked distinctions compared to those in adulthood. This study aimed ...