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Pediatric Radiology|January 1, 1990
Lethal short-rib with median cleft and without polydactyly: a fourth caseL van Maldergem, Y Gillerot, E Salmin, et al.
Clinical Genetics|November 1, 1990
Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritanceL Van Maldergem, Y Gillerot, M Godhaird, et al.
American Journal of Medical Genetics|January 15, 1992
Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome)A Verloes, Y Gillerot, E Walczak, et al.
Acta Clinica Belgica|January 1, 1990
Bradycardia in a case of type II glycogenosis (Pompe's disease) revealing in early neonatal periodL Van Maldergem, D Haumont, D Saurty, et al.
Clinical Genetics|January 1, 1992
Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?L van Maldergem, C Wetzburger, A Verloes, et al.
American Journal of Medical Genetics|May 15, 1993
Oral-facial-digital syndrome type I in a newborn maleY Gillerot, M Heimann, C Fourneau, et al.
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Arterial tortuosity syndrome: case reportC Karakurt, G Koçak, O Elkiran, et al.
Annales De Genetique|January 1, 1989
Roberts-SC phocomelia syndrome with exencephalyA Verloes, C Herens, L Van Maldergem, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1993
[Ophthalmological manifestations of infantile Refsum's disease: apropos of 3 cases]V Van der Maren, M Cordonnier, L Van Maldergem, et al.
Obstetrics and Gynecology|March 1, 1990
Nonimmune hydrops fetalis associated with genetic abnormalitiesE Jauniaux, L Van Maldergem, C De Munter, et al.
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