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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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Cataract, hypertrichosis, and mental retardation (CAHMR): a new autosomal recessive syndrome

S A Temtamy1, A H Sinbawy

  • 1Department of Human Genetics, National Research Center, Cairo, Egypt.

American Journal of Medical Genetics
|December 15, 1991
PubMed

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