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Neuropediatrics|June 25, 1998
Impaired visual perceptual performance on an object recognition task in children with cerebral visual impairmentP Stiers, P De Cock, E VandenbusscheBrain & Development|September 16, 1999
Separating visual perception and non-verbal intelligence in children with early brain injuryP Stiers, P De Cock, E VandenbusscheAmerican Journal of Medical Genetics. Part A|June 10, 2003
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsPhilippe Debeer, H Peeters, S Driess, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23)B Dimitrov, K Devriendt, N M C Maas, et al.American Journal of Medical Genetics|September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Personality profiles of youngsters with velo-cardio-facial syndromeP Prinzie, A Swillen, A Vogels, et al.Genetic Counseling (Geneva, Switzerland)|January 24, 2004
Floating-Harbor syndrome in two sisters: autosomal recessive inheritance or germinal mosaicism?D M Ioan, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Inverted nipples in Robinow syndromeM H Lorenzetti, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Symbrachydactyly in Turner's syndromeL De Smet, J P FrynsAnnales De Genetique|January 1, 1994
Lens dislocation and optic nerve hypoplasia in ring chromosome 21 mosaicismF M Meire, J P FrynsPageof 90