Alain Verloes

New syndrome: clavicle hypoplasia, facial dysmorphism, severe myopia, single central incisor and peripheral neuropathy.

A. Verloes, S. Lesenfants, Alain Verloes, 2001, Clinical dysmorphology.

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.

Coloboma, mental retardation, hypogonadism, and obesity: critical review of the so-called Biemond syndrome type 2, updated nosology, and delineation of three "new" syndromes.

A. Verloes, I. Temple, A. Bottani, 1997, American journal of medical genetics.

Holoprosencephaly and postaxial polydactyly with normal chromosomes. Another observation of a new malformation syndrome; a case report.

Alain Verloes, J. Fryns, Eric Legius, 1990, European journal of obstetrics, gynecology, and reproductive biology.

[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.