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Browsing by Author Smeets, D.

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Full TextIssue DateTitleAuthor(s)
1996Anesthesiologic problems in Williams syndrome : the CACNL2A locus is not involvedMammi, I.; Iles, D.E.; Smeets, D., et al
2008Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.Bon, B.W.M. van; Koolen, D.A.; Borgatti, R., et al
2012A cytogenetic study in a large population of intellectually disabled Indonesians.Mundhofir, F.E.P.; Winarni, T.I.; Bon, B.W.M. van, et al
2011Evaluation of Registration Methods on Thoracic CT: The EMPIRE10 ChallengeMurphy, K.; Ginneken, B. van; Reinhardt, J.M., et al
2012Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversionMundhofir, F.E.; Smeets, D.; Nillesen, W., et al
1997Quality guidelines and standards for genetic laboratories/clinics in prenatal diagnosis on fetal samples obtained by invasive procedures : An attempt to establish a common European framework for quality assessmentMetaxotou, C.; Genuardi, M.; Piombo, G., et al
Showing results 1 to 6 of 6

 

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