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Community Genetics|June 5, 2004
Study of 224 cases of oligohydramnios and congenital malformations in a series of 225,669 consecutive birthsC Stoll, Y Alembik, M P Roth, et al.American Journal of Human Genetics|July 1, 1993
Transforming growth factor-alpha: characterization of the BamHI, RsaI, and TaqI polymorphic regionsJ F Qian, J Feingold, C Stoll, et al.Genetic Counseling (Geneva, Switzerland)|December 3, 2015
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIAC Stoll, Y Alembik, B Dott, et al.Archives Francaises De Pediatrie|March 1, 1987
[Congenital malformations in a series of 66,068 consecutive births]M P Roth, B Dott, Y Alembik, et al.Prenatal Diagnosis|November 1, 1985
Prenatal diagnosis of hypochondroplasiaC Stoll, P Manini, J Bloch, et al.Journal of Medical Genetics|May 1, 1991
Epidemiological and genetic study in 207 cases of oral clefts in Alsace, north-eastern FranceC 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.Nouvelle Revue Francaise D'Hematologie|January 1, 1976
[Clinics and genetics of Glanzmann's thrombasthenia (author's translation)]J M Lévy, C Stoll, A Gardea, et al.Archives Francaises De Pediatrie|June 1, 1975
[Reverse type of cri du chat disease: 5 p trisomy]C Stoll, M O Rethore, C Laurent, et al.Pageof 106