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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 22, 2014
Activation of the chromosome 19q microRNA cluster in sporadic and androgenetic-biparental mosaicism-associated hepatic mesenchymal hamartomaRaj P Kapur, Jessica E Berry, Karen D Tsuchiya, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 23, 2012
Chronic myelogenous leukemia presenting in blast phase with nodal, bilineal myeloid sarcoma and T-lymphoblastic lymphoma in a childXueyan Chen, Joe C Rutledge, David Wu, et al.
Cancer Cell International|May 30, 2006
Cytogenetic characterization and H-ras associated transformation of immortalized human mammary epithelial cellsKrishna Rao, Ozge Alper, Kent E Opheim, et al.
Molecular Cytogenetics|May 13, 2008
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridizationKaren D Tsuchiya, Kent E Opheim, Mark C Hannibal, et al.
Carcinogenesis|June 17, 2003
Extended lifespan of Barrett's esophagus epithelium transduced with the human telomerase catalytic subunit: a useful in vitro modelM Corinna A Palanca-Wessels, Aloysius Klingelhutz, Brian J Reid, et al.
British Journal of Haematology|November 18, 2003
Progenitor cell involvement is predictive of response to induction chemotherapy in paediatric acute myeloid leukaemiaDonna L Johnston, Soheil Meshinchi, Kent E Opheim, et al.
Human Genetics|December 14, 2006
A case of true hermaphroditism reveals an unusual mechanism of twinningVivienne L Souter, Melissa A Parisi, Dale R Nyholt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2007
A Gender Assessment Team: experience with 250 patients over a period of 25 yearsMelissa A Parisi, Linda A Ramsdell, Mark W Burns, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
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