Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
2002 2
2003 2
2005 2
2006 2
2009 2
2012 3
2013 4
2014 7
2015 5
2018 4
2019 1
2020 1
2021 1
2022 2
2023 5
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

42 results

Results by year

Filters applied: . Clear all
Page 1
Trisomies.
Levy PA, Marion R. Levy PA, et al. Among authors: marion r. Pediatr Rev. 2018 Feb;39(2):104-106. doi: 10.1542/pir.2016-0198. Pediatr Rev. 2018. PMID: 29437136 No abstract available.
Contiguous Gene Syndromes.
Pereira E, Marion R. Pereira E, et al. Among authors: marion r. Pediatr Rev. 2018 Jan;39(1):46-49. doi: 10.1542/pir.2016-0073. Pediatr Rev. 2018. PMID: 29292292 Review. No abstract available.
Corrigendum.
Osterbur ML, Zheng R, Marion R, Walsh C, McDonald TV. Osterbur ML, et al. Among authors: marion r. Hum Mutat. 2019 Mar;40(3):357. doi: 10.1002/humu.23711. Hum Mutat. 2019. PMID: 30740826 No abstract available.
The Glycogen Storage Disorders.
Marion RW, Paljevic E. Marion RW, et al. Pediatr Rev. 2020 Jan;41(1):41-44. doi: 10.1542/pir.2018-0146. Pediatr Rev. 2020. PMID: 31894075 Review. No abstract available.
Chromosome 22q11.2 deletion syndrome.
Pereira E, Marion R. Pereira E, et al. Among authors: marion r. Pediatr Rev. 2015 Jun;36(6):270-2; discussion 272. doi: 10.1542/pir.36-6-270. Pediatr Rev. 2015. PMID: 26034260 No abstract available.
Hepatoblastoma in a mosaic trisomy 18 patient.
Pereira EM, Marion R, Ramesh KH, Kim JS, Ewart M, Ricafort R. Pereira EM, et al. Among authors: marion r. J Pediatr Hematol Oncol. 2012 May;34(4):e145-8. doi: 10.1097/MPH.0b013e3182459ee8. J Pediatr Hematol Oncol. 2012. PMID: 22469941 Review.
Diversity in genetic counseling: strategies from the LEND network.
Hatchel A, Willis J, Reiser C, Marion R, Pariseau C, Vanner-Nicely L, Bodurtha J. Hatchel A, et al. Among authors: marion r. J Genet Couns. 2009 Apr;18(2):195-6. doi: 10.1007/s10897-008-9204-x. Epub 2009 Feb 19. J Genet Couns. 2009. PMID: 19225874 No abstract available.
42 results