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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 28, 2009
Concurrent course of transient neonatal diabetes with cholestasis and paucity of interlobular bile ducts: a case reportAlan P Kenny, Nancy A Crimmins, Deborah J G Mackay, et al.
European Journal of Medical Genetics|April 29, 2014
Clinical utility of whole-exome sequencing in rare diseases: GalactosialidosisCarlos E Prada, Claudia Gonzaga-Jauregui, Rebecca Tannenbaum, et al.
Molecular Genetics and Metabolism|November 8, 2015
The management and treatment of children with Fabry disease: A United States-based perspectiveRobert J Hopkin, John L Jefferies, Dawn A Laney, et al.
Pediatric Neurology|January 29, 2019
CNTNAP1-Related Congenital Hypomyelinating NeuropathyHarry Lesmana, Marissa Vawter Lee, Seyed Ali Hosseini, et al.
The American Journal of Cardiology|May 29, 2017
Arrhythmia and Clinical Cardiac Findings in Children With Anderson-Fabry DiseaseHunter C Wilson, Robert J Hopkin, Peace C Madueme, et al.
Fetal Diagnosis and Therapy|September 25, 2009
Severe micrognathia: indications for EXIT-to-AirwayLee M Morris, Foong-Yen Lim, Ravindhra G Elluru, et al.
The Journal of Pediatrics|October 15, 2011
Pediatric plexiform neurofibromas: impact on morbidity and mortality in neurofibromatosis type 1Carlos E Prada, Fatima A Rangwala, Lisa J Martin, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|July 24, 2014
Cost analysis of mandibular distraction versus tracheostomy in neonates with Pierre Robin sequenceChristopher M Runyan, Armando Uribe-Rivera, Audrey Karlea, et al.
Prenatal Diagnosis|August 9, 2014
Predictive value of fetal lung volume in prenatally diagnosed skeletal dysplasiaK Nicole Weaver, Jodie Johnson, Beth Kline-Fath, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 22, 2004
Association of anterior glottic webs with velocardiofacial syndrome (chromosome 22q11.2 deletion)R Christopher Miyamoto, Robin T Cotton, Alan F Rope, et al.
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