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Clinical Genetics|September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his motherC Stoll, P Talon, L Mengus, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Severe hypernatremic dehydration in an infant with Netherton syndromeC Stoll, Y Alembik, D Tchomakov, et al.
Annales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.
Archives Francaises De Pediatrie|February 1, 1992
[Fragile X chromosome in autism and psychotic disorders in children]C Bursztejn, Y Alembik, C Stoll, et al.
Annales De Genetique|January 1, 1995
Distribution of single organ malformations in European populations. EUROCAT Working GroupC Stoll, S Ayme, R Beckers, et al.
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