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The Journal of Pediatrics|August 5, 2006
Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesityJennifer Miller, John Kranzler, Yijun Liu, et al.
Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
Biochemical and Biophysical Research Communications|December 9, 2009
Intermolecular cross-talk between NTR1 and NTR2 neurotensin receptor promotes intracellular sequestration and functional inhibition of NTR1 receptorsJae Ryoung Hwang, Min Woo Baek, Jeonggu Sim, et al.
Hormones & Cancer|December 23, 2019
The Thyroid Hormone Receptor-RUNX2 Axis: A Novel Tumor Suppressive Pathway in Breast CancerEric L Bolf, Noelle E Gillis, Michael S Barnum, et al.
The Journal of Rheumatology|December 1, 1996
Risk factors for adult Still's diseaseJ S Sampalis, T A Medsger, J F Fries, et al.
Human Mutation|August 30, 2008
Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridizationDaniela del Gaudio, Yaping Yang, Barbara A Boggs, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2012
Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?Weimin Bi, Caroline Borgan, Amber N Pursley, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 4, 2008
Efficient, long-term hepatic gene transfer using clinically relevant HDAd doses by balloon occlusion catheter delivery in nonhuman primatesNicola Brunetti-Pierri, Gary E Stapleton, Mark Law, et al.
Human Gene Therapy|August 2, 2013
Transgene expression up to 7 years in nonhuman primates following hepatic transduction with helper-dependent adenoviral vectorsNicola Brunetti-Pierri, Thomas Ng, David Iannitti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2012
Incidental copy-number variants identified by routine genome testing in a clinical populationPhilip M Boone, Zachry T Soens, Ian M Campbell, et al.
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