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Browsing by Author Stankiewicz, P.

Full Text	Issue Date	Title	Author(s)
	2011	The phenotype of recurrent 10q22q23 deletions and duplications	Bon, B.W. van; Balciuniene, J.; Fruhman, G.; Nagamani, S.C.; Broome, D.L., et al
	2009	Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.	Vissers, L.E.L.M.; Bhatt, S.S.; Janssen, I.M.; Xia, Z.; Lalani, S.R., et al
	2007	Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.	Vissers, L.E.L.M.; Stankiewicz, P.; Yatsenko, S.A.; Crawford, E.; Creswick, H., et al
	2007	Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndrome.	Schlaubitz, S.; Yatsenko, S.A.; Smith, L.D.; Keller, K.L.; Vissers, L.E.L.M., et al