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Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Radial ray deficiency and ulnar ray deficiency in two sibsL De Smet, G Fabry, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Symbrachydactyly involving hands and feetL De Smet, G Fabry, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Progressive anterior vertebral body fusion, overgrowth and distinct craniofacial appearanceJ P Fryns, G Fabry, J Remans, 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.Clinical Genetics|January 1, 1988
Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasiasJ P Fryns, G Hofkens, G Fabry, et al.Clinical Dysmorphology|October 25, 2000
A young female with asymmetric manifestations of larsen syndrome: another example of unilateral somatic cell-line mosaicismS G Frints, L De Smet, G Fabry, et al.American Journal of Medical Genetics|January 1, 1979
Brief clinical report: the Dubowitz syndrome in a teenagerJ P Fryns, G Fabry, F Willemyns, et al.European Journal of Pediatrics|September 1, 1980
Deletion of the short arm of chromosome 9. A clinically recognisable entityJ P Fryns, J C Pedersen, H Duyck, et al.Acta Orthopaedica Belgica|August 3, 2002
Genes and orthopedics: from gene to clinic and vice versaPh Debeer, L De Smet, W J M Van De Ven, et al.Genetic Counseling (Geneva, Switzerland)|January 5, 2001
MCA/MR syndrome with severe pre- and postnatal growth retardation, deep mental retardation, distinct facial appearance with nasal hypoplasia, cleft palate and retino-choroidal coloboma in two unrelated female patientsJ P FrynsPageof 97