Showing results (261-270 of 883) with videos related to
Sort By:
Pageof 89
Clinical Genetics|June 1, 1994
Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocationE Smeets, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1991
The 48,XXYY syndrome. Follow-up data on clinical characteristics and psychological findings in 4 patientsM Borghgraef, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the childD Soekarman, J P Fryns, H van den BergheEuropean Journal of Pediatrics|November 4, 1977
The Greig polysyndactyly-craniofacial dysmorphism syndromeJ P Fryns, W Coeck, H van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndromeM Borghgraef, J P Fryns, H Van Den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?J P Fryns, A Vogels, H van den BergheClinical Genetics|February 1, 1990
Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndromeJ P Fryns, A Vogels, H van den BergheClinical Genetics|October 27, 1998
Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletionT Lukusa, K Devriendt, M Holvoet, et al.Genetic Counseling (Geneva, Switzerland)|February 12, 2002
Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school ageA Swillen, K Devriendt, P Ghesquière, et al.Pageof 89