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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.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.European Journal of Clinical Pharmacology|January 1, 1989
Acetylator phenotype and congenital malformationsC Stoll, M P Roth, B Dott, et al.Annales De Genetique|October 17, 2002
Impact of prenatal diagnosis on livebirth prevalence of children with congenital anomaliesClaude Stoll, Y Alembik, B Dott, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22C Stoll, B Roy-Doray, B Dott, et al.Annales De Genetique|April 6, 2002
Evaluation and evolution during time of prenatal diagnosis of congenital heart diseases by routine fetal ultrasonographic examinationC Stoll, B Dott, Y Alembik, et al.Community Genetics|June 5, 2004
Study of 290 cases of polyhydramnios and congenital malformations in a series of 225,669 consecutive birthsC G Stoll, M P Roth, B Dott, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Mental retardation, ataxia, seizures, dysmorphia, and hydrocephaly in two sibs. Angelman syndrome or new syndromeC Stoll, Y Alembik, B Dott, et al.Journal of Medical Genetics|April 1, 1984
Trisomy 1q24----1q41 in two sibs with an insertion in an inverted chromosome 4C Stoll, M P Roth, B DottPageof 33