Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion Journal:American Journal of Medical Genetics, Part A | 2013 | ||
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis Journal:American Journal of Human Genetics | 2011 | ||
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus Journal:American Journal of Human Genetics | 2012 |