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Margaret P Adam

university of washington
H指数:45
被引数:1.0万

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An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome

HNRNPK特异的DNA甲基化特征解释了错义变异,并扩展了Au-Kline综合征的表型谱。

2025-08-070
OA
Implementation of First-Tier Rapid Genome Sequencing in Non-Critical Care Pediatric Wards

在非重症监护儿科病房中实施一级快速基因组测序

2025-06-230
OA
Maternal and paternal risk factors associated with diagnoses within the continuum of fetal alcohol spectrum disorders in the USA: Proximal and distal influences
2024-12-120
PRE
Biallelic PI4KA Mutations Disrupt B-Cell Metabolism and Cause B-Cell Lymphopenia and Hypogammaglobulinemia

双等位基因PI4KA突变破坏b细胞代谢并导致b细胞淋巴细胞减少和低丙种球蛋白血症

2024-09-231
PRE
The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human disease
MED
IF11.8
2023-12-013
OA
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies
2023-05-016
OAAI
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome
2022-10-0117
OAAI
Estimating the community prevalence, child traits, and maternal risk factors of fetal alcohol spectrum disorders (FASD) from a random sample of school children
2021-10-0131
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
Targeted long-read sequencing identifies missing disease-causing variation
2021-08-01137
OAAI
A dyadic approach to the delineation of diagnostic entities in clinical genomics
2021-01-0183
OAAI
The Impact of Rapid Exome Sequencing on Medical Management of Critically III Children
2020-11-0137
OAAI