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Prenatal Diagnosis|April 1, 1992
Evaluation of prenatal diagnosis by a registry of congenital anomaliesC Stoll, Y Alembik, B Dott, et al.Archives Francaises De Pediatrie|October 1, 1991
[Congenital malformations in a series of 131,760 consecutive births during 10 years]C Stoll, B Dott, Y Alembik, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Twelve cases with hemihypertrophy: etiology and follow upC Stoll, Y Alembik, J P Steib, et al.American Journal of Medical Genetics|February 15, 1992
Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?C Stoll, J R Kieny, B Dott, et al.Genetic Epidemiology|January 1, 1988
HLA and Down syndrome (DS): parents at the origin of the nondisjunction share no more HLA-A and -B antigens with their DS child than controlsC Stoll, Y Alembik, N Armbruster, et al.Prenatal Diagnosis|June 1, 1993
Evaluation of prenatal diagnosis of congenital heart diseaseC Stoll, Y Alembik, B Dott, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Are some multiple congenital anomalies with mental retardation (MCA/MR) the clinical expression of rare autosomal fragile sites?C Stoll, C Bolender, A Geraudel, et al.European Journal of Epidemiology|September 1, 1989
Risk factors in congenital heart diseaseC Stoll, Y Alembik, M P Roth, et al.Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) geneC Stoll, M Fischbach, J Terzic, et al.Revue Francaise De Gynecologie Et D'Obstetrique|January 1, 1990
[Maternal oligo-elements and fetal malformations]C Stoll, R Zawislak, B Dott, et al.Pageof 30