A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome is a research paper published in Genes (2022). On theSindex it has a DataRank of 0. It has been cited 1 time.
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NICHD NIH HHS
Grant: P01 HD070454
NIH and the Charles E.H. Upham chair in Pediatrics
Grant: GM125757
National Institutes of Health
Grant: 3R01GM125757-06S1
Molecular Dissection of the 22q11.2 Deletion Syndrome
National Institutes of Health
Grant: 5P01HD070454-05
Mouse Models of Human Conotruncal Defects
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