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Annales De Genetique|August 26, 1998
Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the motherJ P Fryns, E Smeets, K Devriendt, et al.Annales De Genetique|August 26, 1998
Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotypeG Van Buggenhout, L De Coen, J P FrynsClinical Genetics|March 1, 1997
Prenatal growth retardation, microphthalmos/iris coloboma, cloudy cornea, urogenital anomalies and microcephaly. A possible new sublethal syndromeJ P Fryns, H Verresen, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Progressive anterior vertebral body fusion, overgrowth and distinct craniofacial appearanceJ P Fryns, G Fabry, J Remans, et al.American Journal of Medical Genetics|March 1, 1988
Hyperlaxity in males with Melnick-Needles syndromeJ P Fryns, A Schinzel, H Van den BergheGenetic Counseling (Geneva, Switzerland)|June 21, 2008
The long term evolution of 6 adult patients with Cohen syndrome and their behavioral characteristicsK Peeters, D Willekens, J Steyaert, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Behavioral and emotional problems in youngsters with Prader-Willi syndromeL M Curfs, F C Verhulst, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Intelligence and the fra(X) syndrome: a reviewL M Curfs, A M Wiegers, J P FrynsJournal of Mental Deficiency Research|August 1, 1988
Psychological findings in three children with ring 15 chromosomeM Borghgraef, J P Fryns, H Van den BergheEuropean Journal of Pediatrics|December 1, 1986
Internal male pseudohermaphroditism in a 6 week old childT Lukusa, J P Fryns, H Van den BerghePageof 89