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
1967 1
1974 1
1975 2
1979 1
1982 3
1983 1
1985 1
1986 1
1987 3
1989 1
1990 1
1991 3
1992 5
1993 4
1994 2
1995 3
1996 2
1997 4
1998 2
1999 3
2000 3
2001 2
2002 1
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

50 results

Results by year

Filters applied: . Clear all
Page 1
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.
Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D. Warburton PE, et al. Among authors: van hemel jo. Am J Hum Genet. 2000 Jun;66(6):1794-806. doi: 10.1086/302924. Epub 2000 Apr 24. Am J Hum Genet. 2000. PMID: 10777715 Free PMC article. Review.
Paracentric inversion inv(11)(q21q23) in The Netherlands.
Madan K, Pieters MH, Kuyt LP, van Asperen CJ, de Pater JM, Hamers AJ, Gerssen-Schoorl KB, Hustinx TW, Breed AS, Van Hemel JO, et al. Madan K, et al. Among authors: van hemel jo. Hum Genet. 1990 Jun;85(1):15-20. doi: 10.1007/BF00276319. Hum Genet. 1990. PMID: 2358301
Partial trisomy 10q: a recognizable syndrome.
Klep-de Pater JM, Bijlsma JB, de France HF, Leschot NJ, Duijndam-van den Berge M, van Hemel JO. Klep-de Pater JM, et al. Among authors: van hemel jo. Hum Genet. 1979 Jan 19;46(1):29-40. doi: 10.1007/BF00278899. Hum Genet. 1979. PMID: 429004
Etiological studies of severe or familial hypospadias.
Boehmer AL, Nijman RJ, Lammers BA, de Coninck SJ, Van Hemel JO, Themmen AP, Mureau MA, de Jong FH, Brinkmann AO, Niermeijer MF, Drop SL. Boehmer AL, et al. Among authors: van hemel jo. J Urol. 2001 Apr;165(4):1246-54. J Urol. 2001. PMID: 11257695
Genetic counselling before intracytoplasmic sperm injection.
In't Veld PA, Halley DJ, van Hemel JO, Niermeijer MF, Dohle G, Weber RF. In't Veld PA, et al. Among authors: van hemel jo. Lancet. 1997 Aug 16;350(9076):490. doi: 10.1016/s0140-6736(05)63078-4. Lancet. 1997. PMID: 9274588 No abstract available.
50 results