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American Journal of Medical Genetics|September 24, 2002
Facial features in Alagille syndrome: specific or cholestasis facies?Binita M Kamath, Kathleen M Loomes, Rebecca J Oakey, et al.
American Journal of Medical Genetics|September 24, 2002
Characterization of Notch receptor expression in the developing mammalian heart and liverKathleen M Loomes, Darren B Taichman, Curtis L Glover, et al.
Bone|July 16, 2016
Jagged1 expression by osteoblast-lineage cells regulates trabecular bone mass and periosteal expansion in miceD W Youngstrom, M I Dishowitz, C B Bales, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 7, 2019
Hepatic Encephalopathy in Children With Acute Liver Failure: Utility of Serum NeuromarkersNicole A Toney, Michael J Bell, Steven H Belle, et al.
American Journal of Medical Genetics. Part A|June 29, 2012
Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): a review of 53 CdLS pregnanciesDinah M Clark, Ilana Sherer, Matthew A Deardorff, et al.
Hepatology (Baltimore, Md.)|April 1, 2018
Indeterminate pediatric acute liver failure is uniquely characterized by a CD103<sup>+</sup> CD8<sup>+</sup> T-cell infiltrateCatherine A Chapin, Thomas Burn, Tomas Meijome, et al.
British Journal of Pharmacology|October 22, 2011
Pharmacological characterization of rat amylin receptors: implications for the identification of amylin receptor subtypesR J Bailey, C S Walker, A H Ferner, et al.
The Journal of Clinical Investigation|June 11, 2009
Murine Jagged1/Notch signaling in the second heart field orchestrates Fgf8 expression and tissue-tissue interactions during outflow tract developmentFrances A High, Rajan Jain, Jason Z Stoller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2020
Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test resultsRamakrishnan Rajagopalan, Melissa A Gilbert, Deborah A McEldrew, et al.
American Journal of Medical Genetics. Part A|December 25, 2015
Compound heterozygous mutations in NEK8 in siblings with end-stage renal disease with hepatic and cardiac anomaliesRamakrishnan Rajagopalan, Christopher M Grochowski, Melissa A Gilbert, et al.
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