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American Journal of Medical Genetics|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, K Devriendt, A Swillen, et al.Human Genetics|October 6, 1998
Missense mutation and hexanucleotide duplication in the PAX2 gene in two unrelated families with renal-coloboma syndrome (MIM 120330)K Devriendt, G Matthijs, B Van Damme, et al.American Journal of Medical Genetics. Part A|May 20, 2004
Psychotic disorders in Prader-Willi syndromeA Vogels, M De Hert, M J Descheemaeker, et al.Cancer Genetics and Cytogenetics|July 1, 1983
5q- anomaly in a patient with disseminated teratomaG Tricot, J P Fryns, J Thomas, et al.European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|April 18, 2001
Pulmonary sequestration: a comparison between pediatric and adult patientsD Van Raemdonck, K De Boeck, H Devlieger, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|October 1, 1983
Thrombosis of the right umbilical artery, presumably related to the shortness of the umbilical cord: an unusual cause of fetal distressH Devlieger, P Moerman, J Lauweryns, et al.Annals of Neurology|October 23, 1997
The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigreesS Claes, K Devriendt, L Lagae, et al.American Journal of Medical Genetics|December 18, 2001
Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic herniaI Witters, E Legius, P Moerman, et al.European Journal of Medical Genetics|December 28, 2005
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD)Ph Debeer, H Van Esch, C Huysmans, et al.Pageof 105