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European Journal of Pediatrics|August 1, 1997
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletionK E Chandler, C E de Die-Smulders, J J Engelen, et al.Journal of Medical Genetics|November 2, 1999
Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?U Moog, P Maroteaux, C T Schrander-Stumpel, et al.European Journal of Pediatrics|August 1, 1993
Cow's milk protein intolerance in infants under 1 year of age: a prospective epidemiological studyJ J Schrander, J P van den Bogart, P P Forget, et al.American Journal of Medical Genetics. Part A|August 25, 2004
A patient with a de novo 15q24q26.1 interstitial deletion, developmental delay, mild dysmorphism, and very blue irisesL Spruijt, J J M Engelen, I P Bruinen-Smeijsters, et al.European Journal of Pediatrics|June 1, 1994
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patientsC Schrander-Stumpel, P Meinecke, G Wilson, et al.Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Trisomy 7p: report of 2 patients and literature reviewY H Arens, A Toutain, J J Engelen, et al.Clinical Genetics|September 1, 1996
Deletion of the long arm of chromosome 6: two new patients and literature reviewL J Evers, C T Schrander-Stumpel, J J Engelen, et al.Allergy|August 5, 2004
Determinants of neonatal IgE level: parity, maternal age, birth season and perinatal essential fatty acid status in infants of atopic mothersC J A W van Gool, C Thijs, P C Dagnelie, et al.Pageof 2