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L

Lot Snijders Blok

Department of Human Genetics
H指数:15
被引数:1,400

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BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes

BRCA1-、BRCA2-和PALB2相关的范可尼贫血:扩展疾病表型特征并预测杂合子乳腺癌风险的潜力

2025-10-300
PRE
DDX3X-related neurodevelopmental disorder in males - presenting a new cohort of 19 males and a literature review
2025-03-010
OA
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder
2023-01-017
OAAI
Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome
2022-06-0114
OA
Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype

NSD2的功能缺失和错义变异导致甲基化活性降低,并与不同的发育表型相关

2021-08-0132
OAAI
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities

干扰FOXP4转录阻遏物活性的杂合变异导致发育障碍,伴有言语/语言延迟和多种先天性异常

2021-03-0118
OAAI
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

突变特异性病理生理机制定义与SATB1功能障碍相关的不同神经发育障碍

2021-02-0132
OAAI
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
2020-10-0124
OAAI
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome
2020-06-0130
OAAI
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development
NEURON
IF15
2020-05-01132
OAAI
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder
2019-08-0133
OAAI
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)
2019-05-021
OAAI
Mutation update for the SATB2 gene
2019-04-2544
OAAI
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)
2019-02-150
OAAI
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
2018-11-0575
OAAI
NBEA: Developmental disease gene with early generalized epilepsy phenotypes
2018-10-2544
OAAI
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
2015-08-01220
OAAI