Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome-Reference-Cited by-同舟云学术

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Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome

Published:2004-05-01 Issue:5 Volume:41 Page:381-386
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Pinson L

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 61 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum;Cell Stem Cell;2024-06

2. Absence of the RING domain inMID1results in patterning defects in the developing human brain;Life Science Alliance;2024-01-18

3. It’s a TRIM-endous view from the top: the varied roles of TRIpartite Motif proteins in brain development and disease;Frontiers in Molecular Neuroscience;2023-12-05

4. Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant;Molecular Genetics & Genomic Medicine;2023-07-27

5. ARID1B controls transcriptional programs of axon projection in the human corpus callosum;2023-05-04

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