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Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Unilateral absence of the trapezius and pectoralis major muscle: a variant of Poland syndromePh Debeer, P Brys, L De Smet, et al.Annales De Genetique|January 1, 1992
Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndromeD M Ioan, C Maximilian, A Kleczkowska, et al.Clinical Genetics|February 1, 1990
Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literatureC Schrander-Stumpel, J Schrander, J P Fryns, et al.Journal De Genetique Humaine|September 1, 1989
A "new" epi-metaphyseal skeletal dysplasia in four members of a familyJ P Fryns, F De Bisschop, H Van den BergheHuman Genetics|January 19, 1979
Partial monosomy of the long arm of chromosome 16: a distinct clinical entity?J P Fryns, J Bande-Knops, H Van Den BergheArchives of Pathology & Laboratory Medicine|November 1, 1982
Nonimmunologic hydrops fetalis. A study of ten casesP Moerman, J P Fryns, P Goddeeris, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profileL De Smet, E Legius, G Fabry, et al.Bulletin De La Societe Belge D'Ophtalmologie|November 19, 2003
Heterochromia of the irides and a motility disorder of the oesophagus: a coincidence or a defect during embryogenesis?S Goethals, I Hoffman, K Devriendt, et al.Clinical Dysmorphology|June 3, 2005
Scalp skin lesion in Turner syndrome: more than lymphoedema?A Debeer, E Steenkiste, K Devriendt, et al.Pageof 90