Rebecca L Schaub
Overview
Explore the profile of Rebecca L Schaub including associated specialties, affiliations and a list of published articles.
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4
Citations
49
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Recent Articles
1.
Cody J, Heard P, Crandall A, Carter E, Li J, Hardies L, et al.
Am J Med Genet A
. 2009 Jun;
149A(7):1421-30.
PMID: 19533771
One of our primary goals is to help families who have a child with an 18q deletion anticipate medical issues in order to optimize their child's medical care. To this...
2.
Cody J, Semrud-Clikeman M, Hardies L, Lancaster J, Ghidoni P, Schaub R, et al.
Am J Med Genet A
. 2005 Jul;
137(1):9-15.
PMID: 16007630
Most individuals with constitutional deletions of chromosome 18q have developmental delays, dysmyelination of the brain, and growth failure due to growth hormone deficiency. We monitored the effects of growth hormone...
3.
Schaub R, Hale D, Rose S, Leach R, Cody J
J Clin Endocrinol Metab
. 2005 Jan;
90(4):2259-63.
PMID: 15671099
Chromosome 18q deletions (18q-) are survivable autosomal deletions, having an estimated incidence of one in 40,000 live births. Our long-term goals were to 1) comprehensively define the endocrine phenotype, 2)...
4.
Schaub R, Reveles X, Baillargeon J, Leach R, Cody J
Genet Med
. 2002 Feb;
4(1):15-9.
PMID: 11839953
Purpose: To determine the size and parental origin of the deletion in individuals with 18p- syndrome. Methods: Molecular and fluorescence in situ hybridization analyses of the pericentromeric region of chromosome...