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
1985 1
1986 1
1987 1
1989 1
1990 2
1992 2
1993 1
1994 1
1996 1
1997 2
1998 1
2001 2
2002 1
2003 3
2004 1
2006 3
2007 1
2008 3
2009 1
2010 3
2012 1
2015 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

34 results

Results by year

Filters applied: . Clear all
Page 1
Hardikar syndrome: new features.
Poley JR, Proud VK. Poley JR, et al. Among authors: proud vk. Am J Med Genet A. 2008 Oct 1;146A(19):2473-9. doi: 10.1002/ajmg.a.32266. Am J Med Genet A. 2008. PMID: 18792981
Additional EFNB1 mutations in craniofrontonasal syndrome.
Wallis D, Lacbawan F, Jain M, Der Kaloustian VM, Steiner CE, Moeschler JB, Losken HW, Kaitila II, Cantrell S, Proud VK, Carey JC, Day DW, Lev D, Teebi AS, Robinson LK, Hoyme HE, Al-Torki N, Siegel-Bartelt J, Mulliken JB, Robin NH, Saavedra D, Zackai EH, Muenke M. Wallis D, et al. Among authors: proud vk. Am J Med Genet A. 2008 Aug 1;146A(15):2008-12. doi: 10.1002/ajmg.a.32388. Am J Med Genet A. 2008. PMID: 18627045 Free PMC article. No abstract available.
Students online: learning medical genetics.
Proud VK, Johnson ED, Mitchell JA. Proud VK, et al. Am J Hum Genet. 1993 Mar;52(3):637-42. Am J Hum Genet. 1993. PMID: 8447329 Free PMC article.
Classification of the dysmorphology of pectus excavatum.
Cartoski MJ, Nuss D, Goretsky MJ, Proud VK, Croitoru DP, Gustin T, Mitchell K, Vasser E, Kelly RE Jr. Cartoski MJ, et al. Among authors: proud vk. J Pediatr Surg. 2006 Sep;41(9):1573-81. doi: 10.1016/j.jpedsurg.2006.05.055. J Pediatr Surg. 2006. PMID: 16952594
Family study of the inheritance of pectus excavatum.
Creswick HA, Stacey MW, Kelly RE Jr, Gustin T, Nuss D, Harvey H, Goretsky MJ, Vasser E, Welch JC, Mitchell K, Proud VK. Creswick HA, et al. Among authors: proud vk. J Pediatr Surg. 2006 Oct;41(10):1699-703. doi: 10.1016/j.jpedsurg.2006.05.071. J Pediatr Surg. 2006. PMID: 17011272
Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene.
Tompson SW, Bacino CA, Safina NP, Bober MB, Proud VK, Funari T, Wangler MF, Nevarez L, Ala-Kokko L, Wilcox WR, Eyre DR, Krakow D, Cohn DH. Tompson SW, et al. Among authors: proud vk. Am J Hum Genet. 2010 Nov 12;87(5):708-12. doi: 10.1016/j.ajhg.2010.10.009. Epub 2010 Oct 28. Am J Hum Genet. 2010. PMID: 21035103 Free PMC article.
Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8.
Toydemir RM, Chen H, Proud VK, Martin R, van Bokhoven H, Hamel BC, Tuerlings JH, Stratakis CA, Jorde LB, Bamshad MJ. Toydemir RM, et al. Among authors: proud vk. Am J Med Genet A. 2006 Nov 15;140(22):2387-93. doi: 10.1002/ajmg.a.31495. Am J Med Genet A. 2006. PMID: 17041932
34 results