L. Koulischer

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndrome.

Y. Gillerot, L. Koulischer, J. Fryns, 1992, American journal of medical genetics.

Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees.

L. Koulischer, A. Verloes, N. Sakalihasan, 1995, Journal of vascular surgery.

Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees.

N. Sakalihasan, R. Limet, Alain Verloes, 1995, Journal of Vascular Surgery.

Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature.

L. Koulischer, A. Verloes, M. Gonzalès, 1992, American journal of medical genetics.

[Programs of systematic screening in neonatology. Pharmaco-economic aspects].

R. Schoos, Alain Verloes, Bourguignon Jp, 1998, Revue medicale de Liege.

A prenatal trisomy 21 screening program using alpha-fetoprotein, human chorionic gonadotropin, and free estriol assays on maternal dried blood.

L. Koulischer, A. Verloes, R. Schoos, 1995, American journal of obstetrics and gynecology.

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.

L. Koulischer, A. Verloes, A. Galand, 1992, American journal of medical genetics.

Neural tube defects and omphalocele in trisomy 18

Y. Gillerot, L. Koulischer, L. Maldergem, 1989, Clinical genetics.