Showing results (11-20 of 42) with videos related to
Sort By:
Pageof 5
Clinical Genetics|January 1, 1992
On the variable expression of the Brachmann-de Lange syndromeC de Die-Smulders, P Theunissen, C Schrander-Stumpel, et al.Clinical Dysmorphology|October 1, 1996
Alagille syndrome in a family with duplication 20p11U Moog, J Engelen, J Albrechts, et al.Clinical Genetics|April 1, 1994
Prader-Willi-like phenotype in fragile X syndromeC Schrander-Stumpel, W J Gerver, H Meyer, et al.American Journal of Medical Genetics|September 1, 1990
Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndromeC Schrander-Stumpel, C de Die-Smulders, J P Fryns, et al.Journal of Medical Genetics|August 6, 2002
PTPN11 mutations in LEOPARD syndromeE Legius, C Schrander-Stumpel, E Schollen, et al.Clinical Dysmorphology|October 1, 1994
De la Chapelle dysplasia (atelosteogenesis type II): case report and review of the literature [corrected]C Schrander-Stumpel, M Havenith, E V Linden, et al.American Journal of Medical Genetics|April 1, 1992
MASA syndrome: delineation of the clinical spectrum at prepubertal ageJ P Fryns, C Schrander-Stumpel, C De Die-Smulders, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 25, 2000
Aneurysm of the umbilical vein: case report and review of literatureN Vandevijver, R H Hermans, C C Schrander-Stumpel, et al.American Journal of Medical Genetics|December 15, 1991
Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?A Spaepen, C Schrander-Stumpel, J P Fryns, et al.American Journal of Medical Genetics|May 22, 1995
Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional familiesC Schrander-Stumpel, C Höweler, M Jones, et al.Pageof 5