Salden I[au] - Search Results

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Year	Number of Results
2002	1
2003	1
2004	1
2005	3
2024	0

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Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.

Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Vermeesch JR, et al. Among authors: salden i. Eur J Med Genet. 2005 Jul-Sep;48(3):319-27. doi: 10.1016/j.ejmg.2005.04.018. Eur J Med Genet. 2005. PMID: 16179227

The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.

Van Buggenhout G, Van Ravenswaaij-Arts C, Mc Maas N, Thoelen R, Vogels A, Smeets D, Salden I, Matthijs G, Fryns JP, Vermeesch JR. Van Buggenhout G, et al. Among authors: salden i. Eur J Med Genet. 2005 Jul-Sep;48(3):276-89. doi: 10.1016/j.ejmg.2005.05.005. Eur J Med Genet. 2005. PMID: 16179223

Post-zygotic origin of isochromosome 12p.

de Ravel TJ, Keymolen K, van Assche E, Wittevronghel I, Moerman P, Salden I, Matthijs G, Fryns JP, Vermeesch JR. de Ravel TJ, et al. Among authors: salden i. Prenat Diagn. 2004 Dec 15;24(12):984-8. doi: 10.1002/pd.956. Prenat Diagn. 2004. PMID: 15614858

Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia.

Van Esch H, Dom R, Bex D, Salden I, Caeckebeke J, Wibail A, Borghgraef M, Legius E, Fryns JP, Matthijs G. Van Esch H, et al. Among authors: salden i. Eur J Hum Genet. 2005 Jan;13(1):121-3. doi: 10.1038/sj.ejhg.5201312. Eur J Hum Genet. 2005. PMID: 15483640

Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event.

Vermeesch JR, Thoelen R, Salden I, Raes M, Matthijs G, Fryns JP. Vermeesch JR, et al. Among authors: salden i. J Med Genet. 2003 Aug;40(8):e93. doi: 10.1136/jmg.40.8.e93. J Med Genet. 2003. PMID: 12920085 Free PMC article. No abstract available.

Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant.

Vermeesch JR, Syrrou M, Salden I, Dhondt F, Matthijs G, Fryns JP. Vermeesch JR, et al. Among authors: salden i. J Med Genet. 2002 Nov;39(11):e72. doi: 10.1136/jmg.39.11.e72. J Med Genet. 2002. PMID: 12414834 Free PMC article. No abstract available.

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