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Annales De Genetique|January 9, 1999
A patient with 13q-syndrome with mild mental retardation and with growth retardationC Stoll, Y AlembikGenetic 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 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 DottEuropean Journal of Clinical Pharmacology|January 1, 1989
Acetylator phenotype and congenital malformationsC Stoll, M P Roth, B Dott, et al.Prenatal 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 TruttmannPageof 30