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G

Gholson J. Lyon

Institute for Basic Research in Developmental Disabilities
H指数:52
被引数:1.3万

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Phenotypic variability in female individuals with the NAA10 missense variants p.(L126R), p.(L126V), or p.(F128L) leading to NAA10-related syndrome

携带NAA10错义变异p.(L126R)、p.(L126V)或p.(F128L)的女性个体中与NAA10相关综合征相关的表型变异

2026-04-130
OA
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype

cohesin加载器亚基MAU2的致病性变异是独特的Cornelia de Lange综合征亚型的基础

2026-03-300
OAAI
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders
2025-02-010
OAAI
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework
2023-08-0716
OA
Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome

扩大NAA10-related神经发育综合征和NAA15-related神经发育综合征的表型谱

2023-05-0222
OAAI
Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway
2021-08-067
OA
Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?
2021-05-0417
OA
Synaptic processes and immune-related pathways implicated in Tourette syndrome

与抽动秽语综合征有关的突触过程和免疫相关通路

2021-01-1836
OAAI
Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15 (vol 28, pg 2900, 2019)
2020-02-068
OAAI
PEDIA: prioritization of exome data by image analysis

PEDIA: 通过图像分析对外显子组数据进行优先排序

2019-12-0144
OAAI