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
1997 3
2000 1
2001 2
2002 1
2005 1
2009 1
2010 1
2011 1
2015 1
2017 2
2018 2
2019 2
2020 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

18 results

Results by year

Filters applied: . Clear all
Page 1
Genetic testing.
Pagon RA, Hanson NB, Neufeld-Kaiser W, Covington ML. Pagon RA, et al. Among authors: neufeld kaiser w. West J Med. 2001 May;174(5):344-7. doi: 10.1136/ewjm.174.5.344. West J Med. 2001. PMID: 11342518 Free PMC article. Review. No abstract available.
Genetic consultation.
Pagon RA, Hanson NB, Neufeld-Kaiser W, Covington ML. Pagon RA, et al. Among authors: neufeld kaiser w. West J Med. 2001 Jun;174(6):397-9. doi: 10.1136/ewjm.174.6.397. West J Med. 2001. PMID: 11381007 Free PMC article. No abstract available.
Genetic counseling practice analysis.
Hampel H, Grubs RE, Walton CS, Nguyen E, Breidenbach DH, Nettles S; American Board of Genetic Counseling 2008 Practice Analysis Advisory Committee; Callanan N, Corliss M, Fox S, Hiraki S, Ku L, Neufeld-Kaiser W, Riley B, Taylor J, Weik L. Hampel H, et al. Among authors: neufeld kaiser w. J Genet Couns. 2009 Jun;18(3):205-16. doi: 10.1007/s10897-009-9216-1. Epub 2009 Mar 11. J Genet Couns. 2009. PMID: 19277852
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.
Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium; Dobyns WB, Baas F, Poll-The BT. Namavar Y, et al. Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287. Epub 2010 Oct 15. Brain. 2011. PMID: 20952379 Free PMC article.
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.
Riggs ER, Nelson T, Merz A, Ackley T, Bunke B, Collins CD, Collinson MN, Fan YS, Goodenberger ML, Golden DM, Haglund-Hazy L, Krgovic D, Lamb AN, Lewis Z, Li G, Liu Y, Meck J, Neufeld-Kaiser W, Runke CK, Sanmann JN, Stavropoulos DJ, Strong E, Su M, Tayeh MK, Kokalj Vokac N, Thorland EC, Andersen E, Martin CL. Riggs ER, et al. Among authors: neufeld kaiser w. Hum Mutat. 2018 Nov;39(11):1650-1659. doi: 10.1002/humu.23610. Hum Mutat. 2018. PMID: 30095202 Free PMC article.
18 results