Getting to the heart of DiGeorge syndrome

This publication has 9 references indexed in Scilit:

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• Congenital heart disease in mice deficient for the DiGeorge syndrome region
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• A common molecular basis for rearrangement disorders on chromosome 22q11
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• Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11
  American Journal of Human Genetics, 1999
• A Molecular Pathway Revealing a Genetic Basis for Human Cardiac and Craniofacial Defects
  Science, 1999
• HIRA, a DiGeorge Syndrome Candidate Gene, Is Required for Cardiac Outflow Tract Septation
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• Frequency of 22q11 deletions in patients with conotruncal defects
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• Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization
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• Neural Crest and Cardiovascular Patterning
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