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Items: 13

1.

Health Supervision for Children With Neurofibromatosis Type 1.

Miller DT, Freedenberg D, Schorry E, Ullrich NJ, Viskochil D, Korf BR; COUNCIL ON GENETICS; AMERICAN COLLEGE OF MEDICAL GENETICS AND GENOMICS.

Pediatrics. 2019 May;143(5). pii: e20190660. doi: 10.1542/peds.2019-0660. Review.

PMID:
31010905
2.

Survey of family history taking and genetic testing in pediatric practice.

Saul RA, Trotter T, Sease K, Tarini B.

J Community Genet. 2017 Apr;8(2):109-115. doi: 10.1007/s12687-016-0291-3. Epub 2017 Jan 7.

3.

The childless man.

Scheuerle AE, Picconi JL, Neidich J, Panny S, Plecher BA, Randolph LM, Trapane P, Trotter TL.

Am J Med Genet A. 2014 Feb;164A(2):561. doi: 10.1002/ajmg.a.36290. Epub 2013 Dec 5. No abstract available.

PMID:
24311465
4.

Primary care and genetics and genomics.

Scott J, Trotter T.

Pediatrics. 2013 Dec;132(Suppl 3):S231-7. doi: 10.1542/peds.2013-1032H.

PMID:
24298132
5.

Effective communication of molecular genetic test results to primary care providers.

Scheuner MT, Edelen MO, Hilborne LH, Lubin IM; RAND Molecular Genetic Test Report Advisory Board.

Genet Med. 2013 Jun;15(6):444-9. doi: 10.1038/gim.2012.151. Epub 2012 Dec 6.

PMID:
23222660
6.

A report template for molecular genetic tests designed to improve communication between the clinician and laboratory.

Scheuner MT, Hilborne L, Brown J, Lubin IM; members of the RAND Molecular Genetic Test Report Advisory Board.

Genet Test Mol Biomarkers. 2012 Jul;16(7):761-9. doi: 10.1089/gtmb.2011.0328. Epub 2012 Jun 25.

PMID:
22731646
7.

Secretary's Advisory Committee on Heritable Disorders in Newborns and Children response to the President's Council on Bioethics report: the changing moral focus of newborn screening.

Trotter TL, Fleischman AR, Howell RR, Lloyd-Puryear M; Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.

Genet Med. 2011 Apr;13(4):301-4. doi: 10.1097/GIM.0b013e318210655d. No abstract available.

PMID:
21407080
8.

Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children.

Calonge N, Green NS, Rinaldo P, Lloyd-Puryear M, Dougherty D, Boyle C, Watson M, Trotter T, Terry SF, Howell RR; Advisory Committee on Heritable Disorders in Newborns and Children.

Genet Med. 2010 Mar;12(3):153-9. doi: 10.1097/GIM.0b013e3181d2af04.

PMID:
20154628
10.

Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report.

Lubin IM, McGovern MM, Gibson Z, Gross SJ, Lyon E, Pagon RA, Pratt VM, Rashid J, Shaw C, Stoddard L, Trotter TL, Williams MS, Amos Wilson J, Pass K.

J Mol Diagn. 2009 Mar;11(2):162-71. doi: 10.2353/jmoldx.2009.080130. Epub 2009 Feb 5.

11.

Ordering molecular genetic tests and reporting results: practices in laboratory and clinical settings.

Lubin IM, Caggana M, Constantin C, Gross SJ, Lyon E, Pagon RA, Trotter TL, Wilson JA, McGovern MM.

J Mol Diagn. 2008 Sep;10(5):459-68. doi: 10.2353/jmoldx.2008.080050. Epub 2008 Jul 31.

12.

Family history in pediatric primary care.

Trotter TL, Martin HM.

Pediatrics. 2007 Sep;120 Suppl 2:S60-5. Review.

PMID:
17767006
13.

Health supervision for children with achondroplasia.

Trotter TL, Hall JG; American Academy of Pediatrics Committee on Genetics.

Pediatrics. 2005 Sep;116(3):771-83. Erratum in: Pediatrics. 2005 Dec;116(6):1615.

PMID:
16140722

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