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Genetic 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 Obstetrics and Gynecology|September 1, 1991
Study of 156 cases of polyhydramnios and congenital malformations in a series of 118,265 consecutive birthsC G Stoll, Y Alembik, B DottPrenatal Diagnosis|September 22, 1998
Evaluation of prenatal diagnosis of congenital heart diseaseC Stoll, Y Alembik, B Dott, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parentsC Stoll, Y Alembik, P LutzGenetic Counseling (Geneva, Switzerland)|January 1, 1997
On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant geneY Alembik, C Stoll, J MesserAnnales De Genetique|January 1, 1996
Multiple familial lipomatosis with polyneuropathy, an inherited dominant conditionC Stoll, Y Alembik, M TruttmannGenetic Counseling (Geneva, Switzerland)|July 17, 1998
Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girlC Stoll, Y Alembik, M RepettoGenetic Counseling (Geneva, Switzerland)|July 17, 1998
Sporadic case of dyssegmental dysplasia with antenatal presentationC Stoll, B Langer, B Gasser, et al.Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Wiedemann-Rautenstrauch syndrome. A case report and review of the literatureC Stoll, F Labay, J Geisert, et al.Pageof 33