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Journal De Genetique Humaine|September 1, 1985
[Correlations between pregnancy pathology, study of the placenta, antenatal echography and examination of the product of conception in a series of 175 congenital malformations]C Stoll, P Curie, 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.Revue Francaise De Gynecologie Et D'Obstetrique|January 1, 1990
[Oligo-elements of the amniotic fluid from normal, hypotrophic and trisomy 21 fetuses]C Stoll, B Dott, E A Maier, et al.Journal of Medical Genetics|December 1, 1980
Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15)C Stoll, J Levy, M P RothCancer Research|August 1, 1982
Sister chromatid exchange and growth kinetics in chronic myeloid leukemiaC Stoll, F Oberling, M P RothGenetic 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.Journal De Genetique Humaine|September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]C Stoll, M P Roth, J M LevyPrenatal Diagnosis|November 1, 1985
Prenatal diagnosis of hypochondroplasiaC Stoll, P Manini, J Bloch, 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.Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Severe hypernatremic dehydration in an infant with Netherton syndromeC Stoll, Y Alembik, D Tchomakov, et al.Pageof 33