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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
2024 0

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50 results

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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.
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.
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
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
Familial occurrence of the g syndrome.
van Biervliet JP, van Hemel JO. van Biervliet JP, et al. Among authors: van hemel jo. Clin Genet. 1975 Mar;7(3):238-44. doi: 10.1111/j.1399-0004.1975.tb00325.x. Clin Genet. 1975. PMID: 1139793
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
50 results