Robert F Stratton
Overview
Explore the profile of Robert F Stratton including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
174
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0
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Recent Articles
1.
Cody J, Hasi M, Soileau B, Heard P, Carter E, Sebold C, et al.
Hum Genet
. 2013 Oct;
133(2):199-209.
PMID: 24092497
Although constitutional chromosome abnormalities have been recognized since the 1960s, clinical characterization and development of treatment options have been hampered by their obvious genetic complexity and relative rarity. Additionally, deletions...
2.
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...
3.
Probst F, Roeder E, Enciso V, Ou Z, Cooper M, Eng P, et al.
Am J Med Genet A
. 2007 May;
143A(12):1358-65.
PMID: 17506108
Chromosomal microarray analysis (CMA) by array-based comparative genomic hybridization (CGH) is a new clinical test for the detection of well-characterized genomic disorders caused by chromosomal deletions and duplications that result...
4.
Cody J, Sebold C, Malik A, Heard P, Carter E, Crandall A, et al.
Am J Med Genet A
. 2007 May;
143A(11):1181-90.
PMID: 17486614
Most deletions of the long arm of chromosome 18 involve some part of the most distal 30 Mb. We have identified five individuals with cytogenetically diagnosed interstitial deletions that are...
5.
Ming J, Kaupas M, Roessler E, Brunner H, Golabi M, Tekin M, et al.
Hum Genet
. 2002 Apr;
110(4):297-301.
PMID: 11941477
Holoprosencephaly (HPE) is the most commonly occurring congenital structural forebrain anomaly in humans. HPE is associated with mental retardation and craniofacial malformations. The genetic causes of HPE have recently begun...