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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

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Gorlin-goltz syndrome: case report of a rare hereditary disorder

Ashutosh Agrawal1, Aditi Murari, Sunil Vutukuri

  • 1Department of Oral Pathology and Microbiology, Institute of Dental Sciences, Uttar Pradesh, Bareilly 243006, India.

Case Reports in Dentistry
|October 11, 2012
PubMed

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