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
1978 1
1981 2
1982 2
1984 1
1985 1
1987 1
1988 3
1989 2
1990 5
1991 1
1992 10
1993 5
1994 9
1995 9
1996 16
1997 4
1998 9
1999 15
2000 11
2001 7
2002 13
2003 4
2004 10
2005 9
2006 9
2007 7
2008 5
2009 13
2010 7
2011 9
2012 12
2013 5
2014 4
2015 1
2017 2
2018 1
2019 4
2020 3
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

218 results

Results by year

Filters applied: . Clear all
Page 1
Ehlers-Danlos syndrome.
Hamel BC. Hamel BC. Neth J Med. 2004 May;62(5):140-2. Neth J Med. 2004. PMID: 15366695 Free article. No abstract available.
X-linked mental retardation.
Ropers HH, Hamel BC. Ropers HH, et al. Among authors: hamel bc. Nat Rev Genet. 2005 Jan;6(1):46-57. doi: 10.1038/nrg1501. Nat Rev Genet. 2005. PMID: 15630421 Review.
Craniofrontonasal dysplasia.
Kapusta L, Brunner HG, Hamel BC. Kapusta L, et al. Among authors: hamel bc. Eur J Pediatr. 1992 Nov;151(11):837-41. doi: 10.1007/BF01957936. Eur J Pediatr. 1992. PMID: 1468459
Oculocerebrocutaneous syndrome.
Bleeker-Wagemakers LM, Hamel BC, Hennekam RC, Beemer FA, Oorthuys HW. Bleeker-Wagemakers LM, et al. Among authors: hamel bc. J Med Genet. 1990 Jan;27(1):69-70. doi: 10.1136/jmg.27.1.69. J Med Genet. 1990. PMID: 2407849 Free PMC article. Review. No abstract available.
Acrocallosal syndrome.
Hendriks HJ, Brunner HG, Haagen TA, Hamel BC. Hendriks HJ, et al. Among authors: hamel bc. Am J Med Genet. 1990 Mar;35(3):443-6. doi: 10.1002/ajmg.1320350325. Am J Med Genet. 1990. PMID: 2309796
[Polydactyly].
Nicolai JP, Hamel BC, Menalda GA. Nicolai JP, et al. Among authors: hamel bc. Ned Tijdschr Geneeskd. 1990 Jan 27;134(4):157-9. Ned Tijdschr Geneeskd. 1990. PMID: 2304571 Dutch. No abstract available.
Compound-heterozygous Marfan syndrome.
Van Dijk FS, Hamel BC, Hilhorst-Hofstee Y, Mulder BJ, Timmermans J, Pals G, Cobben JM. Van Dijk FS, et al. Among authors: hamel bc. Eur J Med Genet. 2009 Jan-Feb;52(1):1-5. doi: 10.1016/j.ejmg.2008.11.004. Epub 2008 Nov 27. Eur J Med Genet. 2009. PMID: 19059503
The p63 gene in EEC and other syndromes.
Brunner HG, Hamel BC, Van Bokhoven H. Brunner HG, et al. Among authors: hamel bc. J Med Genet. 2002 Jun;39(6):377-81. doi: 10.1136/jmg.39.6.377. J Med Genet. 2002. PMID: 12070241 Free PMC article. Review.
P63 gene mutations and human developmental syndromes.
Brunner HG, Hamel BC, Bokhoven Hv Hv. Brunner HG, et al. Among authors: hamel bc. Am J Med Genet. 2002 Oct 15;112(3):284-90. doi: 10.1002/ajmg.10778. Am J Med Genet. 2002. PMID: 12357472 Review.
218 results