Zobrazeno 1 - 4
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pro vyhledávání: '"Sridevi Abboy"'
Publikováno v:
Journal of Genetic Counseling. 27:1411-1416
Medullary thyroid carcinoma (MTC) is often due to the hereditary condition multiple endocrine neoplasia type 2 (MEN2) and it is standard of care to offer genetic testing to all diagnosed patients. This study used the Kaiser Permanente integrated medi
Publikováno v:
Familial Cancer. 17:175-178
The introduction of screening for multiple high and moderate risk mutations in genes has resulted in a complex approach to patient care involving multiple disciplines. We sought to describe the feasibility of a single visit multidisciplinary approach
Autor:
Jeanne Meck, Kavita S. Reddy, Harold N. Bass, George E. Tiller, Swaroop Aradhya, Sridevi Abboy
Publikováno v:
Genetics in Medicine. 15:3-13
A small supernumerary marker chromosome is often seen in patients with developmental disorders. Prior to array-based comparative genomic hybridization markers were rarely genotyped end to end. In this study, a valid genotype-to-phenotype correlation
Autor:
Emily Parkhurst, Sridevi Abboy
Publikováno v:
Journal of pediatric ophthalmology and strabismus. 53(6)
Purpose: To examine the incidence, presentation, and outcome of optic gliomas in children with neurofibromatosis type 1 (NF1) in Southern California Kaiser Permanente. Methods: The authors queried the Southern California Kaiser Permanente electronic