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Submitted by admin on June 23, 2011 - 3:08pm
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Biblio
Found 2 results
2005
Hur DJ, Raymond GV, Kahler SG, Riegert-Johnson DL, Cohen BA, Boyadjiev SA.
2005. A novel MGP mutation in a consanguineous family: review of the clinical and molecular characteristics of Keutel syndrome.. American journal of medical genetics. Part A. 135(1):36-40. Abstract
Boyadjiev SA, South ST, Radford CL, Patel A, Zhang G, Hur DJ, Thomas GH, Gearhart JP, Stetten G.
2005. A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.. Genomics. 85(5):622-9. Abstract

