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Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
No evidence for genomic imprinting in liver-born Down syndrome patientsC Stoll, Y Alembik, B Dott, et al.Annales De Genetique|May 20, 2000
Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examinationC Stoll, B Dott, Y Alembik, et al.Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Sporadic case of dyssegmental dysplasia with antenatal presentationC Stoll, B Langer, B Gasser, et al.Reproductive Toxicology (Elmsford, N.Y.)|March 18, 1999
Maternal trace elements, vitamin B12, vitamin A, folic acid, and fetal malformationsC Stoll, B Dott, Y Alembik, 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.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Familial cylindromatosisC Stoll, Y Alembik, A Wilk, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Arthrogryposis, ectodermal dysplasia and other anomalies in two sistersC Stoll, Y Alembik, S Finck, et al.Annales De Genetique|April 24, 1999
Congenital anomalies associated with congenital hypothyroidismC Stoll, B Dott, Y Alembik, et al.American Journal of Medical Genetics|January 1, 1994
Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive birthsC Stoll, Y Alembik, B Dott, et al.Journal De Genetique Humaine|December 1, 1989
[Anomalies in thyroid function in children with trisomy 21]C Stoll, Y Alembik, B Dott, et al.Pageof 29