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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 Berghe
Genetic 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 Berghe
Genetic 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 Berghe
European Journal of Pediatrics|November 4, 1977
The Greig polysyndactyly-craniofacial dysmorphism syndromeJ P Fryns, W Coeck, H van den Berghe
Genetic 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 Berghe
Genetic 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 Berghe
Human Genetics|April 15, 1977
Y to X translocation in manH van den Berghe, P Petit, J P Fryns
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.
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