Showing results (81-90 of 291) with videos related to
Sort By:
Pageof 30
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Severe hypernatremic dehydration in an infant with Netherton syndromeC Stoll, Y Alembik, D Tchomakov, et al.Annales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.European 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.Archives Francaises De Pediatrie|February 1, 1992
[Fragile X chromosome in autism and psychotic disorders in children]C Bursztejn, Y Alembik, C Stoll, et al.American 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 DottAnnales De Genetique|October 17, 2002
Impact of prenatal diagnosis on livebirth prevalence of children with congenital anomaliesClaude Stoll, Y Alembik, B Dott, 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.Clinical Dysmorphology|February 2, 2002
Shprintzen-Goldberg marfanoid syndrome: a case followed up for 24 yearsC StollAmerican Journal of Medical Genetics|April 12, 2001
Problems in the diagnosis of fragile X syndrome in young children are still presentC StollPageof 30