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Inverted duplication of 22pter----q11.21 in cat-eye syndrome.
Hoo JJ, Robertson A, Fowlow SB, Bowen P, Lin CC. Hoo JJ, et al. Among authors: fowlow sb. Am J Med Genet. 1986 Jul;24(3):543-5. doi: 10.1002/ajmg.1320240320. Am J Med Genet. 1986. PMID: 3728573 No abstract available.
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.
Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ, Whiteman DA, et al. Weksberg R, et al. Among authors: fowlow sb. Hum Mol Genet. 1993 May;2(5):549-56. doi: 10.1093/hmg/2.5.549. Hum Mol Genet. 1993. PMID: 8518793
Autosomal recessive juvenile cataract in Hutterites.
Pearce WG, Mackay JA, Holmes TM, Morgan K, Fowlow SB, Shokeir MH, Lowry RB. Pearce WG, et al. Among authors: fowlow sb. Ophthalmic Paediatr Genet. 1987 Jun;8(2):119-24. doi: 10.3109/13816818709028527. Ophthalmic Paediatr Genet. 1987. PMID: 3658338
11 results