Fryns JP - Search Results

1

Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism.

Robberecht C, Voet T, Utine GE, Schinzel A, de Leeuw N, Fryns JP, Vermeesch J. Robberecht C, et al. Among authors: fryns jp. Mol Cytogenet. 2012 Apr 10;5:19. doi: 10.1186/1755-8166-5-19. Mol Cytogenet. 2012. PMID: 22490612 Free PMC article.

2

Piecing together the problems in diagnosing low-level chromosomal mosaicism.

Robberecht C, Fryns JP, Vermeesch JR. Robberecht C, et al. Among authors: fryns jp. Genome Med. 2010 Jul 29;2(7):47. doi: 10.1186/gm168. Genome Med. 2010. PMID: 20670383 Free PMC article.

3

Chromosome instability is common in human cleavage-stage embryos.

Vanneste E, Voet T, Le Caignec C, Ampe M, Konings P, Melotte C, Debrock S, Amyere M, Vikkula M, Schuit F, Fryns JP, Verbeke G, D'Hooghe T, Moreau Y, Vermeesch JR. Vanneste E, et al. Among authors: fryns jp. Nat Med. 2009 May;15(5):577-83. doi: 10.1038/nm.1924. Epub 2009 Apr 26. Nat Med. 2009. PMID: 19396175 Free article.

4

Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.

Robberecht C, Schuddinck V, Fryns JP, Vermeesch JR. Robberecht C, et al. Among authors: fryns jp. Genet Med. 2009 Sep;11(9):646-54. doi: 10.1097/GIM.0b013e3181abc92a. Genet Med. 2009. PMID: 19617844 Free article.

5

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate.

Vanneste E, Voet T, Melotte C, Debrock S, Sermon K, Staessen C, Liebaers I, Fryns JP, D'Hooghe T, Vermeesch JR. Vanneste E, et al. Among authors: fryns jp. Hum Reprod. 2009 Nov;24(11):2679-82. doi: 10.1093/humrep/dep266. Epub 2009 Jul 24. Hum Reprod. 2009. PMID: 19633308 Free PMC article.

6

Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies.

Nowakowska BA, de Leeuw N, Ruivenkamp CA, Sikkema-Raddatz B, Crolla JA, Thoelen R, Koopmans M, den Hollander N, van Haeringen A, van der Kevie-Kersemaekers AM, Pfundt R, Mieloo H, van Essen T, de Vries BB, Green A, Reardon W, Fryns JP, Vermeesch JR. Nowakowska BA, et al. Among authors: fryns jp. Eur J Hum Genet. 2012 Feb;20(2):166-70. doi: 10.1038/ejhg.2011.157. Epub 2011 Sep 14. Eur J Hum Genet. 2012. PMID: 21915152 Free PMC article.

7

Cytogenetic and morphological analysis of early products of conception following hystero-embryoscopy from couples with recurrent pregnancy loss.

Robberecht C, Pexsters A, Deprest J, Fryns JP, D'Hooghe T, Vermeesch JR. Robberecht C, et al. Among authors: fryns jp. Prenat Diagn. 2012 Oct;32(10):933-42. doi: 10.1002/pd.3936. Epub 2012 Jul 4. Prenat Diagn. 2012. PMID: 22763612

8

Chromosome healing of constitutional chromosome deletions studied by microdissection.

Vermeesch JR, Falzetti D, Van Buggenhout G, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: fryns jp. Cytogenet Cell Genet. 1998;81(1):68-72. doi: 10.1159/000014991. Cytogenet Cell Genet. 1998. PMID: 9691179

9

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly.

Dimitrov BI, Voet T, De Smet L, Vermeesch JR, Devriendt K, Fryns JP, Debeer P. Dimitrov BI, et al. Among authors: fryns jp. J Med Genet. 2010 Aug;47(8):569-74. doi: 10.1136/jmg.2009.073833. Epub 2010 Jul 7. J Med Genet. 2010. PMID: 20610440

10

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos.

Voet T, Vanneste E, Van der Aa N, Melotte C, Jackmaert S, Vandendael T, Declercq M, Debrock S, Fryns JP, Moreau Y, D'Hooghe T, Vermeesch JR. Voet T, et al. Among authors: fryns jp. Hum Mutat. 2011 Jul;32(7):783-93. doi: 10.1002/humu.21502. Hum Mutat. 2011. PMID: 21412953

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