Truncation ofNHEJ1 in a patient with polymicrogyria-Reference-Cited by-同舟云学术

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Truncation ofNHEJ1 in a patient with polymicrogyria

Published:2007 Issue:4 Volume:28 Page:356-364
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Cantagrel Vincent,Lossi Anne-Marie,Lisgo Steven,Missirian Chantal,Borges Ana,Philip Nicole,Fernandez Carla,Cardoso Carlos,Figarella-Branger Dominique,Moncla Anne,Lindsay Susan,Dobyns William B.,Villard Laurent

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference44 articles.

1. XLF Interacts with the XRCC4-DNA Ligase IV Complex to Promote DNA Nonhomologous End-Joining

2. Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

3. Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals

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1. Brain Malformations;Keeling's Fetal and Neonatal Pathology;2022

2. Neuropathology of genetically defined malformations of cortical development—A systematic literature review;Neuropathology and Applied Neurobiology;2021-02-14

3. Combined deletions of IHH and NHEJ1 cause chondrodystrophy and embryonic lethality in the Creeper chicken;Communications Biology;2020-03-25

4. An immunocompetent patient with a nonsense mutation in NHEJ1 gene;BMC Medical Genetics;2019-03-21

5. The Subplate: A Potential Driver of Cortical Folding?;Cerebral Cortex;2019-02-04

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