Engelen JJ - Search Results

1

Subtelomeric chromosome aberrations: still a lot to learn.

Moog U, Arens YH, van Lent-Albrechts JC, Huijts PE, Smeets EE, Schrander-Stumpel CT, Engelen JJ. Moog U, et al. Among authors: engelen jj. Clin Genet. 2005 Nov;68(5):397-407. doi: 10.1111/j.1399-0004.2005.00506.x. Clin Genet. 2005. PMID: 16207207

2

Characterization of a chromosome 8-derived minute marker chromosome using microdissection and FISH in a boy with growth retardation.

Engelen JJ, Schrander-Stumpel CT, Theunissen PM, Vaes-Peeters G, Albrechts JC, Hamers AJ. Engelen JJ, et al. Am J Med Genet A. 2003 Apr 30;118A(3):274-8. doi: 10.1002/ajmg.a.10267. Am J Med Genet A. 2003. PMID: 12673659

3

Intrachromosomal insertion translocation resulting in duplication of chromosome band Yq11.2 in two fertile brothers.

Engelen JJ, Arens YH, Gondrie ET, Alofs MG, Loneus WH, Hamers AJ. Engelen JJ, et al. Am J Med Genet A. 2003 Apr 30;118A(3):287-9. doi: 10.1002/ajmg.a.10203. Am J Med Genet A. 2003. PMID: 12673661

4

Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.

Engelen JJ, Moog U, Weber J, Haagen AA, van Uum CM, Hamers AJ. Engelen JJ, et al. Am J Med Genet A. 2003 Jun 15;119A(3):356-9. doi: 10.1002/ajmg.a.10266. Am J Med Genet A. 2003. PMID: 12784305

5

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers.

Arens YH, Engelen JJ, Govaerts LC, van Ravenswaay CM, Loneus WH, van Lent-Albrechts JC, van der Blij-Philipsen M, Hamers AJ, Schrander-Stumpel CT. Arens YH, et al. Among authors: engelen jj. Am J Med Genet A. 2004 Oct 1;130A(2):128-33. doi: 10.1002/ajmg.a.20568. Am J Med Genet A. 2004. PMID: 15372532

6

Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.

Moog U, Engelen JJ, de Die-Smulders CE, Albrechts JC, Loneus WH, Haagen AA, Raven EJ, Hamers AJ. Moog U, et al. Among authors: engelen jj. Clin Genet. 1994 Dec;46(6):423-9. doi: 10.1111/j.1399-0004.1994.tb04410.x. Clin Genet. 1994. PMID: 7889659 Review.

7

Marker chromosome identification by micro-FISH.

Engelen JJ, Loots WJ, Motoh PC, Moog U, Hamers GJ, Geraedts JP. Engelen JJ, et al. Clin Genet. 1996 May;49(5):242-8. doi: 10.1111/j.1399-0004.1996.tb03781.x. Clin Genet. 1996. PMID: 8832132

8

Deletion of the long arm of chromosome 6: two new patients and literature review.

Evers LJ, Schrander-Stumpel CT, Engelen JJ, Hoorntje TM, Pulles-Heintzberger CF, Schrander JJ, Albrechts JC, Peters J, Fryns JP. Evers LJ, et al. Among authors: engelen jj. Clin Genet. 1996 Sep;50(3):138-44. doi: 10.1111/j.1399-0004.1996.tb02368.x. Clin Genet. 1996. PMID: 8946112

9

Duplication of chromosome region 8p23.1-->p23.3: a benign variant?

Engelen JJ, Moog U, Evers JL, Dassen H, Albrechts JC, Hamers AJ. Engelen JJ, et al. Am J Med Genet. 2000 Mar 6;91(1):18-21. Am J Med Genet. 2000. PMID: 10751083

10

Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplications.

Moog U, Engelen JJ, Albrechts JC, Baars LG, de Die-Smulders CE. Moog U, et al. Among authors: engelen jj. Am J Med Genet. 2000 Oct 2;94(4):306-10. doi: 10.1002/1096-8628(20001002)94:4<306::aid-ajmg8>3.0.co;2-v. Am J Med Genet. 2000. PMID: 11038444 Review.

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