ChrisSullivanMD

Physician

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PubMed

57 citations
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
Samin A. Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun
Plos Genetics. 2013-10-03
53 citations
Deletion 16p13.11 uncovers NDE1 mutations on the non‐deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption
Alex R. Paciorkowski, Kim M. Keppler-Noreuil, Luther K. Robinson, Christopher T. Sullivan, Samin A. Sajan
American Journal of Medical Genetics. Part A. 2013-07-01
18 citations
X Chromosome-Inactivation Patterns in 31 Individuals with PHACE Syndrome
C.T. Sullivan, Susan L. Christian, Joseph T. Shieh, Denise W. Metry, Francine Blei
Molecular Syndromology. 2012-11-16

Hospitals Need More IT: ReportSeptember 17th, 2021
Seven-in-10 Hospital Executives Acknowledge Need to Invest More to Maximize Staff EfficiencySeptember 15th, 2021
Majority of Hospital Executives Acknowledge the Need to Invest More to Maximize Staff EfficiencySeptember 15th, 2021
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