Significados de unrelated patients en inglés

The molecular analyses were performed in a group of 50 unrelated patients.

Patients and results: We report four unrelated patients with ACC and SDHx mutations.

We describe two unrelated patients referred to two different institutions for investigation of thrombocytopenia.

Forty-two unrelated patients mostly originating from Western China were recruited.

Definitive proof of pathogenicity will require confirmation in unrelated patients.

Direct sequencing of EpCAM from 2 additional unrelated patients revealed novel mutations in the gene.

This report describes two unrelated patients with obesity, mental retardation, body asymmetry, and muscle weakness.

Case report: Two unrelated patients presented with slowly progressive or nonprogressive proximal muscle weakness since childhood.

Participants and methods: Two unrelated patients with confirmed SARS-CoV-2 infection and bilateral acute conjunctivitis were examined.

We report on two unrelated patients with a proximal deletion of the long arm of chromosome 21.

We now report somatic SMAD3 mutations in bone lesions of four unrelated patients with endosteal pattern melorheostosis.

Out of 273 unrelated patients, only 3 subjects had defects in FAM161A.

Methods: Mutational analysis of KCNJ2 was performed for 541 unrelated patients.

We used DHPLC to scan mutations in these genes in a cohort of unrelated patients with C282Y mutation.

Here we report the germline and somatic findings for two unrelated patients with NF1 and high-grade serous OC.

The other 2 unrelated patients participated in studies for undiagnosed pediatric hyperkinetic movement disorders and underwent whole-exome sequencing.