WT1 GENE PRODUCT

\dˌʌbə͡ljˌuːtˈiː wˈɒn d͡ʒˈiːn pɹˈɒdʌkt], \dˌʌbə‍ljˌuːtˈiː wˈɒn d‍ʒˈiːn pɹˈɒdʌkt], \d_ˌʌ_b_əl_j_ˌuː_t_ˈiː w_ˈɒ_n dʒ_ˈiː_n p_ɹ_ˈɒ_d_ʌ_k_t]\

Definitions of WT1 GENE PRODUCT

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Acquired Meningomyeloceles

  • Congenital, or rarely acquired, herniation meningeal spinal cord tissue through a bony defect vertebral column. majority these defects occur lumbosacral region. features include PARAPLEGIA, loss of sensation in the lower body, and incontinence. This condition may be associated with ARNOLD-CHIARI MALFORMATION HYDROCEPHALUS. (From Joynt, Clinical Neurology, 1992, Ch55, pp35-6)
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