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Expanding the spectrum of microdeletion 4q21 syndrome: A partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and pierre robin sequence
Authors:Elizabeth Bhoj  Sara Halbach  Donna McDonald‐McGinn  Christopher Tan  Rachel Lande  Darrel Waggoner  Elaine Zackai
Affiliation:1. Division of Genetics, The Children's Hospital of Philadelphia, , Philadelphia, Pennsylvania;2. Department of Human Genetics, University of Chicago, , Chicago, Illinois
Abstract:
Keywords:4q21 microdeletion syndrome  growth delay  PRKG2  SCD5  cleft palate  Pierre Robin sequence  developmental delay  microdeletion  4q21
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