|
Cain, Corey J; Gaborit, Nathalie; Lwin, Wint et al. (2016) Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization. Bone Rep 5:86-95
|
|
Cain, Corey J; Valencia, Joel T; Ho, Samantha et al. (2016) Increased Gs Signaling in Osteoblasts Reduces Bone Marrow and Whole-Body Adiposity in Male Mice. Endocrinology 157:1481-94
|
|
Bershteyn, Marina; Hayashi, Yohei; Desachy, Guillaume et al. (2014) Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells. Nature 507:99-103
|
|
Zayed, Hatem; Chao, Ryan; Moshrefi, Ali et al. (2010) A maternally inherited chromosome 18q22.1 deletion in a male with late-presenting diaphragmatic hernia and microphthalmia-evaluation of DSEL as a candidate gene for the diaphragmatic defect. Am J Med Genet A 152A:916-23
|
|
Mathias, R S; Kostiner, D; Packman, S (2001) Hyperammonemia in urea cycle disorders: role of the nephrologist. Am J Kidney Dis 37:1069-80
|
|
Chen, E; Cleaver, J E; Weber, C A et al. (1994) Trichothiodystrophy: clinical spectrum, central nervous system imaging, and biochemical characterization of two siblings. J Invest Dermatol 103:154S-158S
|
|
Eggerding, F A; Schonberg, S A; Chehab, F F et al. (1994) Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation. Am J Hum Genet 55:253-65
|
|
Cogen, P H; Daneshvar, L; Metzger, A K et al. (1992) Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis. Am J Hum Genet 50:584-9
|
|
Ferrell, L; Schmidt, K; Sheffield, V et al. (1992) Neonatal hemochromatosis: genetic counseling based on retrospective pathologic diagnosis. Am J Med Genet 44:429-33
|
|
Kuller, J A; Hoffman, E P; Fries, M H et al. (1992) Prenatal diagnosis of Duchenne muscular dystrophy by fetal muscle biopsy. Hum Genet 90:34-40
|
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