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American Journal of Medical Genetics|September 1, 1990
Dandy-Walker variant malformation, spastic paraplegia, and mental retardation in two sibsC Stoll, C Huber, Y Alembik, et al.
Archives Francaises De Pediatrie|October 1, 1993
[The MASA syndrome (Mental retardation, Aphasia, Spastic paraplegia and Adducted thumbs), is it heterogeneous?]C Stoll, Y Alembik, M Pfindel, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
An unusual human mosaic for skin pigmentationC Stoll, Y Alembik, E Grosshans, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1984
Discordance for skeletal and cardiac defect in monozygotic twinsC Stoll, M P Roth, B Dott, et al.
Clinical Genetics|March 1, 1986
Usefulness of a registry of congenital malformations for genetic counseling and prenatal diagnosisC Stoll, M P Roth, B Dott, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Twelve cases with hemihypertrophy: etiology and follow upC Stoll, Y Alembik, J P Steib, 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.
American Journal of Medical Genetics|February 1, 1985
Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndromeC Stoll, A Geraudel, H Berland, et al.
Genetic 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.
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