Van Hemel JO - Search Results

1

CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21) (q13.1;q22.3).

De Krijger RR, Mooy CM, Van Hemel JO, Sulkers EJ, Kros JM, Bartelings MM, Govaerts LC. De Krijger RR, et al. Among authors: van hemel jo. Pediatr Dev Pathol. 1999 Nov-Dec;2(6):577-81. doi: 10.1007/s100249900165. Pediatr Dev Pathol. 1999. PMID: 10508883

2

Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14).

de Vries BB, Eussen BH, van Diggelen OP, van Der Heide A, Deelen WH, Govaerts LC, Lindhout D, Wouters CH, Van Hemel JO. de Vries BB, et al. Among authors: van hemel jo. Am J Med Genet. 1999 Nov 19;87(2):189-94. doi: 10.1002/(sici)1096-8628(19991119)87:2<189::aid-ajmg12>3.3.co;2-h. Am J Med Genet. 1999. PMID: 10533035

3

Genetic risk factors in infertile men with severe oligozoospermia and azoospermia.

Dohle GR, Halley DJ, Van Hemel JO, van den Ouwel AM, Pieters MH, Weber RF, Govaerts LC. Dohle GR, et al. Among authors: van hemel jo. Hum Reprod. 2002 Jan;17(1):13-6. doi: 10.1093/humrep/17.1.13. Hum Reprod. 2002. PMID: 11756355 Free article.

4

[Finishing a pregnancy in an infaust fetal prognosis].

Niermeijer MF, Los FJ, Govaerts LC, van Hemel JO, Wouters CH. Niermeijer MF, et al. Among authors: van hemel jo. Ned Tijdschr Geneeskd. 1998 Feb 28;142(9):485. Ned Tijdschr Geneeskd. 1998. PMID: 9562765 Dutch. No abstract available.

5

Avoidance of emergency surgery in newborn infants with trisomy 18.

Bos AP, Broers CJ, Hazebroek FW, van Hemel JO, Tibboel D, Wesby-van Swaay E, Molenaar JC. Bos AP, et al. Among authors: van hemel jo. Lancet. 1992 Apr 11;339(8798):913-5. doi: 10.1016/0140-6736(92)90940-5. Lancet. 1992. PMID: 1348308

6

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.

7

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.

8

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.

9

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.

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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