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J

John C. Carey

Utah System of Higher Education
H指数:81
被引数:2.5万

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RNA sequencing provides functional insights and diagnostic resolution in previously unsolved rare disease cases

RNA测序为先前未解决的罕见病病例提供了功能见解和诊断分辨率。

2025-11-140
OA
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit

Utah NeoSeq项目:一个促进新生儿重症监护室基因组诊断的协作性多学科项目

2025-03-230
OA
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
2022-09-014
OAAI
Response to Biesecker et al.
2021-09-010
OAAI
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

PRKAR1B的变异导致自闭症谱系障碍,失用症和对疼痛不敏感的神经发育障碍

2021-08-0115
OAAI
A dyadic approach to the delineation of diagnostic entities in clinical genomics
2021-01-0183
OAAI
Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variants
2020-08-0133
OAAI
Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2
2019-04-0454
OAAI
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
2019-03-0126
OAAI