Publications by Medical Specialty - Pediatrics
These publications were authored or co-authored by Quest Diagnostics staff.
- Clinical and Lab healthcare professionals
- Endocrinology, Diabetes & Metabolism
- Family medicine practitioners
- General Health and Wellness
- Geriatrics/Age Management
- Health Information Technology
- Infectious Disease
- Internal Medicine
- Nurse practitioners
- Pathology, Anatomic
- Pathology, Laboratory Medicine
- Physician assistants
- Sports Medicine
- Toxicology/Pain Management
- Women's Health/OB/GYN
'Criteria' aPL tests: report of a task force and preconference workshop at the 13th International Congress on Antiphospholipid Antibodies, Galveston, Texas, April 2010.
Authors: Pierangeli SS, de Groot PG, Dlott J, Favaloro E, Harris EN, Lakos G, Ortel T, Meroni PL, Otomo K, Pengo V, Tincani A, Wong R, Roubey R.
Primary and probable secondary dengue virus (DV) infection rates in relation to age among DV IgM-positive patients residing in the United States mainland versus the Caribbean islands.
Authors: Prince HE, Yeh C, Lape-Nixon M.
Clin Vaccine Immunol. 2012;19:105-108.
Trainable immunohistochemical HER2/neu image analysis: a multisite performance study using 260 breast tissue specimens.
Quest Diagnostics Authors: Agersborg, S
Authors: Nassar A, Cohen C, Zhou W, Lynch KA, Albitar M, Barker EA, Vanderbilt BL, Thompson J, Heyman ER, Lange H, Olson A, Siddiqui MT.
Arch Pathol Lab Med. 2011;135:896-902.
Secondary mutation (c.94_95delAG) in A -alpha(3.7) allele associated with Hb H disease in two unrelated African American individuals homozygous for the -alpha(3.7) deletion (-alpha(3.7)/-alpha(3.7T)).
Authors: Zhao P, Buller-Burckle AM, Peng M, Anderson A, Han ZJ, Gallivan MV.
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
Authors: Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, Francina A, Galanello R, Gallivan MV, Georgitsi M, Gibbons RJ, Giordano PC, Harteveld CL, Hoyer JD,
Nat Genet. 2011;43:295-301.
Spectral karyotyping for identification of constitutional chromosomal abnormalities at a national reference laboratory.
Mol Cytogenet. 2012;5:3.