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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.Prenatal Diagnosis|November 1, 1985
Prenatal diagnosis of hypochondroplasiaC Stoll, P Manini, J Bloch, 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.Archives Francaises De Pediatrie|December 1, 1983
[Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression]C Stoll, M P Roth, H Hessemann, et al.Epilepsia|November 1, 1990
Landau-Kleffner syndrome: a pharmacologic study of five casesC Marescaux, E Hirsch, S Finck, et al.Fetal Diagnosis and Therapy|January 1, 1996
Sirenomelia and situs inversus: case report and review of the literatureB Langer, C Stoll, R Nicolau, et al.Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in uteroC Stoll, F Audeoud, C Gaugler, et al.Environmental Science & Technology|August 1, 2012
Prevalence of clinically relevant antibiotic resistance genes in surface water samples collected from Germany and AustraliaC Stoll, J P S Sidhu, A Tiehm, et al.Pageof 30