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Pediatrie|September 1, 1985
[Opsomyoclonus syndrome in children. A new case. Review of the literature (110 cases)]P Talon, C StollAnnales De Genetique|July 18, 2002
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 geneC Stoll, P SauvageAnnales De Genetique|April 24, 1999
A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophyC Stoll, D EyerGenetic Counseling (Geneva, Switzerland)|January 22, 2005
Brachydactyly type E in two sibs with increased bone density and mental retardation. A new autosomal recessive syndrome?C Stoll, Y AlembikGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Oto-palato-digital syndrome type IIC Stoll, Y AlembikGenetic Counseling (Geneva, Switzerland)|January 1, 1994
A boy with neurofibromatosis 1 and Poland anomalyY Alembik, C StollAmerican Journal of Medical Genetics. Part A|September 17, 2004
Do parents and grandparents of patients with achondroplasia have a higher cancer risk?C Stoll, J FeingoldNouvelle Revue Francaise D'Hematologie|January 1, 1982
Y chromosome duplication in chronic myeloid leukemiaC Stoll, F OberlingPageof 46