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Jaap Schrander

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J M A Verhagen; Yvonne J Vos; J W Weber; Jaap Bakker; M M J Blezer; M Estela Rubio-Gozalbo; Jaap J P Schrander; C T R M Schrander-Stumpel; Alexander P A Stegmann; Suzanna G M Frints
Adducted thumbs: a clinical clue to genetic diagnosis.
Aimée D C Paulussen; Alexander P A Stegmann; Marinus J Blok; Demis Tserpelis; Crool Posma-Velter; Yvonne Detisch; Eric E J Smeets; Annemieke Wagemans; Jaap J P Schrander; Marie-José H van den Boogaard; Jasper van der Smagt; Arie van Haeringen; Irene Stolte-Dijkstra; Wilhelmina S Kerstjens-Frederikse; Grazia M Mancini; Marja W Wessels; Raoul C M Hennekam; Maaike Vreeburg; Joep P M Geraedts; T J L de Ravel; Jean-Pierre Fryns; H J M Smeets; koenraad devriendt; Constance T R M Schrander-Stumpel
MLL2 mutation spectrum in 45 patients with Kabuki syndrome.
C T R M Schrander-Stumpel; Margje Sinnema; Lieke van den Hout; Marian A Maaskant; Henny M J van Schrojenstein Lantman-de Valk; Annemieke Wagemans; Jaap J P Schrander; Leopold M G Curfs
Healthcare transition in persons with intellectual disabilities: general issues, the Maastricht model, and Prader-Willi syndrome.

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All Publications

2013: J M A Verhagen; Yvonne J Vos; J W Weber; Jaap Bakker; M M J Blezer; M Estela Rubio-Gozalbo; Jaap J P Schrander; C T R M Schrander-Stumpel; Alexander P A Stegmann; Suzanna G M Frints
Adducted thumbs: a clinical clue to genetic diagnosis.
European journal of medical genetics 2013;56(3):153-8.
2011: Aimée D C Paulussen; Alexander P A Stegmann; Marinus J Blok; Demis Tserpelis; Crool Posma-Velter; Yvonne Detisch; Eric E J Smeets; Annemieke Wagemans; Jaap J P Schrander; Marie-José H van den Boogaard; Jasper van der Smagt; Arie van Haeringen; Irene Stolte-Dijkstra; Wilhelmina S Kerstjens-Frederikse; Grazia M Mancini; Marja W Wessels; Raoul C M Hennekam; Maaike Vreeburg; Joep P M Geraedts; T J L de Ravel; Jean-Pierre Fryns; H J M Smeets; koenraad devriendt; Constance T R M Schrander-Stumpel
MLL2 mutation spectrum in 45 patients with Kabuki syndrome.
Human mutation 2011;32(2):E2018-25.
2007: C T R M Schrander-Stumpel; Margje Sinnema; Lieke van den Hout; Marian A Maaskant; Henny M J van Schrojenstein Lantman-de Valk; Annemieke Wagemans; Jaap J P Schrander; Leopold M G Curfs
Healthcare transition in persons with intellectual disabilities: general issues, the Maastricht model, and Prader-Willi syndrome.
American journal of medical genetics. Part C, Seminars in medical genetics 2007;145C(3):241-7.
2006: Joris G J L de Kort; S G F Robben; Jaap J P Schrander; Lodewijk W van Rhijn
Multifocal osteomyelitis in a child: a rare manifestation of cat scratch disease: a case report and systematic review of the literature.
Journal of pediatric orthopedics. Part B 2006;15(4):285-8.
2005: C T R M Schrander-Stumpel; Liesbeth Spruyt; Leopold M G Curfs; Tom Defloor; Jaap J P Schrander
Kabuki syndrome: Clinical data in 20 patients, literature review, and further guidelines for preventive management.
American journal of medical genetics. Part A 2005;132A(3):234-43.
2004: L Spruijt; J J M Engelen; I P Bruinen-Smeijsters; J C M Albrechts; Jaap J P Schrander; C T R M Schrander-Stumpel
A patient with a de novo 15q24q26.1 interstitial deletion, developmental delay, mild dysmorphism, and very blue irises.
American journal of medical genetics. Part A 2004;129A(3):312-5.
2004: C J A W van Gool; Carel Thijs; Pieter C Dagnelie; Cécile Henquet; Adriana C van Houwelingen; Jaap J P Schrander; Paul P C A Menheere; Piet A van den Brandt
Determinants of neonatal IgE level: parity, maternal age, birth season and perinatal essential fatty acid status in infants of atopic mothers.
Allergy 2004;59(9):961-8.
2004: C T R M Schrander-Stumpel; Leopold M G Curfs; Prapto Sastrowijoto; Suzanne B Cassidy; Jaap J P Schrander; Jean-Pierre Fryns
Prader-Willi syndrome: causes of death in an international series of 27 cases.
American journal of medical genetics. Part A 2004;124A(4):333-8.
2003: C J A W van Gool; Carel Thijs; Cécile Henquet; Adriana C van Houwelingen; Pieter C Dagnelie; Jaap J P Schrander; Paul P C A Menheere; Piet A van den Brandt
Gamma-linolenic acid supplementation for prophylaxis of atopic dermatitis--a randomized controlled trial in infants at high familial risk.
The American journal of clinical nutrition 2003;77(4):943-51.
2002: Henriette ter Heide; Sjoerd K Bulstra; Ad Reekers; Jaap J P Schrander; C T R M Schrander-Stumpel
Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome.
American journal of medical genetics 2002;110(4):359-64.
2000: Y H J M Arens; A Toutain; J J M Engelen; JP Offermans; A J H Hamers; Jaap J P Schrander; CF Pulles-Heintzberger; C T R M Schrander-Stumpel
Trisomy 7p: report of 2 patients and literature review.
Genetic counseling (Geneva, Switzerland) 2000;11(4):347-54.
1999: Ute Moog; P Maroteaux; C T R M Schrander-Stumpel; André Van Ooij; Jaap J P Schrander; Jean-Pierre Fryns
Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?
Journal of medical genetics 1999;36(11):856-8.
1998: Lucien J C Anteunis; P Brienesse; Jaap J P Schrander
Otoacoustic emissions in screening cleft lip and/or palate children for hearing loss--a feasibility study.
International journal of pediatric otorhinolaryngology 1998;44(3):259-66.
1998: C Schaap; M P ten Tusscher; Jaap J P Schrander; R H Kuijten; C T R M Schrander-Stumpel
Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes: are they related?
European journal of pediatrics 1998;157(2):170-1.
1997: K E Chandler; C E M de Die-Smulders; J J M Engelen; Jaap J P Schrander
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
European journal of pediatrics 1997;156(8):636-8.
1996: L J Evers; C T R M Schrander-Stumpel; J J M Engelen; T M Hoorntje; C F Pulles-Heintzberger; Jaap J P Schrander; J C M Albrechts; J Peters; J P Fryns
Deletion of the long arm of chromosome 6: two new patients and literature review.
Clinical genetics 1996;50(3):138-44.
1993: Jaap J P Schrander; J P van den Bogart; P Ph Forget; C T R M Schrander-Stumpel; R H Kuijten; A D Kester
Cow's milk protein intolerance in infants under 1 year of age: a prospective epidemiological study.
European journal of pediatrics 1993;152(8):640-4.
1993: Jaap J P Schrander; J J Dellevoet; Jan-Willem Arends; P Ph Forget; R Kuijten
Small intestinal mucosa IgE plasma cells and specific anti-cow milk IgE in children with cow milk protein intolerance.
Annals of allergy 1993;70(5):406-9.
1992: Jaap J P Schrander; S Oudsen; P Ph Forget; R H Kuijten
Follow up study of cow's milk protein intolerant infants.
European journal of pediatrics 1992;151(10):783-5.
1991: C T R M Schrander-Stumpel; J P Fryns; Jaap J P Schrander; J Vles
Distal arthrogryposis, specific facial dysmorphism and psychomotor retardation: a recognizable entity in surviving patients with the fetal akinesia deformation sequence.
Genetic counseling (Geneva, Switzerland) 1991;2(2):69-75.
1990: Jaap J P Schrander; R W Unsalan-Hooyen; P Ph Forget; J Jansen
[51Cr]EDTA intestinal permeability in children with cow's milk intolerance.
Journal of pediatric gastroenterology and nutrition 1990;10(2):189-92.