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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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14q(22) deletion in a familial case of anophthalmia with polydactyly

M E Ahmad1, Rima Dada, Tanuj Dada

  • 1Genetics Division, Department of Anatomy, All India Institute of Medical Sciences, New Delhi 110029, India.

American Journal of Medical Genetics. Part A
|June 10, 2003
PubMed

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