Geraedts JP - Search Results

1

Marker chromosome identification by micro-FISH.

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

2

Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.

Engelen JJ, Loots WJ, Albrechts JC, Motoh PC, Fryns JP, Hamers AJ, Geraedts JP. Engelen JJ, et al. Among authors: geraedts jp. J Med Genet. 1996 Jul;33(7):562-6. doi: 10.1136/jmg.33.7.562. J Med Genet. 1996. PMID: 8818941 Free PMC article.

3

Application of micro-FISH to delineate deletions.

Engelen JJ, Albrechts JC, Loots WJ, Hollanders-Crombach BH, Hamers AJ, Geraedts JP. Engelen JJ, et al. Among authors: geraedts jp. Cytogenet Cell Genet. 1996;75(2-3):167-71. doi: 10.1159/000134471. Cytogenet Cell Genet. 1996. PMID: 9040786

4

Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.

Engelen JJ, Loots WJ, Albrechts JC, Plomp AS, van der Meer SB, Vles JS, Hamers GJ, Geraedts JP. Engelen JJ, et al. Among authors: geraedts jp. Am J Med Genet. 1998 Feb 3;75(4):409-13. Am J Med Genet. 1998. PMID: 9482648

5

A simple and efficient method for microdissection and microFISH.

Engelen JJ, Albrechts JC, Hamers GJ, Geraedts JP. Engelen JJ, et al. Among authors: geraedts jp. J Med Genet. 1998 Apr;35(4):265-8. doi: 10.1136/jmg.35.4.265. J Med Genet. 1998. PMID: 9598716 Free PMC article.

6

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. Among authors: geraedts jp. Genet Couns. 1999;10(2):123-32. Genet Couns. 1999. PMID: 10422004 Review.

7

Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping.

Meijer H, Hamers GJ, Jongbloed RJ, Vaes-Peeters GP, van der Hulst RR, Geraedts JP. Meijer H, et al. Among authors: geraedts jp. Hum Genet. 1989 Oct;83(3):280-6. doi: 10.1007/BF00285173. Hum Genet. 1989. PMID: 2571564

8

SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations.

van Uum CM, Stevens SJ, Dreesen JC, Drüsedau M, Smeets HJ, Hollanders-Crombach B, Die-Smulders CE, Geraedts JP, Engelen JJ, Coonen E. van Uum CM, et al. Among authors: geraedts jp. Eur J Hum Genet. 2012 Sep;20(9):938-44. doi: 10.1038/ejhg.2012.27. Epub 2012 Feb 29. Eur J Hum Genet. 2012. PMID: 22378284 Free PMC article.

9

Paternal transmission of congenital myotonic dystrophy.

de Die-Smulders CE, Smeets HJ, Loots W, Anten HB, Mirandolle JF, Geraedts JP, Höweler CJ. de Die-Smulders CE, et al. Among authors: geraedts jp. J Med Genet. 1997 Nov;34(11):930-3. doi: 10.1136/jmg.34.11.930. J Med Genet. 1997. PMID: 9391889 Free PMC article.

10

Fluorescence in situ hybridization on paraffin-embedded abortion material as a means of retrospective chromosome analysis.

van Lijnschoten G, Albrechts J, Vallinga M, Hopman AH, Arends JW, Geraedts J. van Lijnschoten G, et al. Hum Genet. 1994 Nov;94(5):518-22. doi: 10.1007/BF00211018. Hum Genet. 1994. PMID: 7959687

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