Search Results - "PRESSMAN, C. L"

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  1. 1

    Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients by SHIMKETS, R, GAILANI, M. R, SIU, V. M, YANG-FENG, T, PRESSMAN, C. L, LEVANAT, S, GOLDSTEIN, A, DEAN, M, BALE, A. E

    Published in American journal of human genetics (01-08-1996)
    “…Gorlin syndrome is an autosomal dominant disorder characterized by multiple basal cell carcinomas, medulloblastomas, ovarian fibromas, and a variety of…”
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    Journal Article
  2. 2

    lmx1b, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye by Pressman, Carolyn L., Chen, Haixu, Johnson, Randy L.

    Published in Genesis (New York, N.Y. : 2000) (01-01-2000)
    “…Proper development of the anterior segment of the mammalian eye is critical for normal ocular function. Indeed, several congenital syndromes associated with…”
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  3. 3

    Multiple calvarial defects in lmx1b mutant mice by Chen, Haixu, Ovchinnikov, Dmitry, Pressman, Carolyn L., Aulehla, Alexander, Lun, Yi, Johnson, Randy L.

    Published in Developmental genetics (1998)
    “…The vertebrate cranial vault, or calvaria, forms during embryonic development from cranial mesenchyme of multiple embryonic origins. Inductive interactions are…”
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