Van Hemel JO - Search Results

1

Ring chromosome 2: clinical, chromosomal, and biochemical aspects.

Jansen M, Beemer FA, van der Heiden C, Van Hemel JO, Van den Brande JL. Jansen M, et al. Among authors: van den brande jl, van der heiden c, van hemel jo. Hum Genet. 1982;60(1):91-5. doi: 10.1007/BF00281274. Hum Genet. 1982. PMID: 7076252

2

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

3

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.

4

Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome.

Van Hemel JO, Eussen B, Wesby-van Swaay E, Oostra BA. Van Hemel JO, et al. Hum Genet. 1992 Mar;88(6):661-7. doi: 10.1007/BF02265294. Hum Genet. 1992. PMID: 1551671 Review.

5

Interchromosomal insertions. Identification of five cases and a review.

Van Hemel JO, Eussen HJ. Van Hemel JO, et al. Hum Genet. 2000 Nov;107(5):415-32. doi: 10.1007/s004390000398. Hum Genet. 2000. PMID: 11140939 Review.

6

De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data.

Los FJ, Van Hemel JO, Jacobs HJ, Drop SL, van Dongen JJ. Los FJ, et al. Among authors: van dongen jj, van hemel jo. J Med Genet. 1994 Jan;31(1):72-3. doi: 10.1136/jmg.31.1.72. J Med Genet. 1994. PMID: 8151644 Free PMC article.

7

A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations.

van Hemel JO, van Biervliet JP, de Jager-van der Grift PW. van Hemel JO, et al. Among authors: van biervliet jp. Clin Genet. 1975 Sep;8(3):213-7. doi: 10.1111/j.1399-0004.1975.tb01496.x. Clin Genet. 1975. PMID: 1175325 No abstract available.

8

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 asperen cj, van hemel jo. Hum Genet. 1990 Jun;85(1):15-20. doi: 10.1007/BF00276319. Hum Genet. 1990. PMID: 2358301

9

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience.

Tuerlings JH, de France HF, Hamers A, Hordijk R, Van Hemel JO, Hansson K, Hoovers JM, Madan K, Van der Blij-Philipsen M, Gerssen-Schoorl KB, Kremer JA, Smeets DF. Tuerlings JH, et al. Among authors: van hemel jo. Eur J Hum Genet. 1998 May-Jun;6(3):194-200. doi: 10.1038/sj.ejhg.5200193. Eur J Hum Genet. 1998. PMID: 9781022

10

Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome.

Wouters CH, Meijers-Heijboer HJ, Eussen BJ, van der Heide AA, van Luijk RB, van Drunen E, Beverloo BB, Visscher F, Van Hemel JO. Wouters CH, et al. Among authors: van hemel jo. Am J Med Genet. 2001 Aug 15;102(3):261-5. doi: 10.1002/ajmg.1468. Am J Med Genet. 2001. PMID: 11484204

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