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Emilie D. Douine

University of California System
H指数:29
被引数:2,350

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The spectrum of heart defects in the TRAF7-related multiple congenital anomalies-intellectual disability syndrome
2024-03-110
OAAI
Characterization of spastic paraplegia in a family with a novel PSEN1 mutation
2023-02-152
OAAI
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling
2022-01-2118
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
KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants (vol 21, 10.1038/s41436-018-0259-2, 2019)
2020-11-010
OAAI
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
2020-05-0124
OAAI
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder (vol 19, pg 238, 2020)
2020-04-013
OAAI
Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

转录组测序对罕见孟德尔疾病的诊断效用

2020-03-01136
OAAI
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

USP9X功能的部分丧失导致男性神经发育和行为障碍收敛于转化生长因子 β 信号传导

2020-01-0149
OAAI
Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis

MYBPC1中的杂合变异与超出关节挛缩的神经肌肉表型相关

2019-05-0522
OAAI
KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants
2019-04-0185
OAAI
Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region

与snao1鸟苷三磷酸结合区相关的神经发育疾病谱

2019-01-2554
OAAI
A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative
2019-01-0162
OAAI
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

扩大BAF相关疾病的范围: SMARCC2的从头变体导致智力障碍和发育迟缓的综合征

2019-01-0163
OAAI