Engelen JJ - Search Results

1

A radiation hybrid map of the X-chromosome of the dog (Canis familiaris).

Everts RE, van Wolferen ME, Versteeg SA, Zijlstra C, Engelen JJ, Bosma AA, Rothuizen J, van Oost BA. Everts RE, et al. Among authors: engelen jj. Cytogenet Genome Res. 2002;98(1):86-92. doi: 10.1159/000068547. Cytogenet Genome Res. 2002. PMID: 12584447

2

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

3

Assignment of the human gene for smoothelin (SMTN) to chromosome 22q12 by fluorescence in situ hybridization and radiation hybrid mapping.

Engelen JJ, Esterling LE, Albrechts JC, Detera-Wadleigh SD, van Eys GJ. Engelen JJ, et al. Genomics. 1997 Jul 15;43(2):245-7. doi: 10.1006/geno.1997.9999. Genomics. 1997. PMID: 9244445 No abstract available.

4

Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.

de Pater J, Van der Sijs-Bos C, Prins M, Derks J, Albrechts J, Engelen J. de Pater J, et al. Eur J Med Genet. 2006 Jul-Aug;49(4):306-12. doi: 10.1016/j.ejmg.2005.12.006. Epub 2006 Jan 19. Eur J Med Genet. 2006. PMID: 16461028

5

Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.

Wanderley HY, Schrander-Stumpel CT, Visser MO, Van Maanen-Op Het Roodt EA, Loneus WH, Engelen JJ. Wanderley HY, et al. Among authors: engelen jj. Genet Couns. 2005;16(3):277-82. Genet Couns. 2005. PMID: 16259325

6

Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.

Knegt AC, Li S, Engelen JJ, Bijlsma EK, Warburton PE. Knegt AC, et al. Among authors: engelen jj. Prenat Diagn. 2003 Mar;23(3):215-20. doi: 10.1002/pd.559. Prenat Diagn. 2003. PMID: 12627422

7

Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH.

Engelen JJ, Tuerlings JH, Albrechts JC, Schrander-Stumpel CT, Hamers AJ, De Die-Smulders CE. Engelen JJ, et al. Genet Couns. 2000;11(1):13-7. Genet Couns. 2000. PMID: 10756422

8

Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18.

de Pater JM, Poot M, Beemer FA, Bijlsma JB, Hack WW, Van Dam WM, Eleveld MJ, Loneus WH, Engelen JJ. de Pater JM, et al. Among authors: engelen jj. Eur J Med Genet. 2006 Jan-Feb;49(1):19-27. doi: 10.1016/j.ejmg.2005.01.005. Epub 2005 Feb 8. Eur J Med Genet. 2006. PMID: 16473306

9

Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.

Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP. Engelen JJ, et al. Genet Couns. 1999;10(2):123-32. Genet Couns. 1999. PMID: 10422004 Review.

10

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

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