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Annales De Genetique|January 9, 1999
A patient with 13q-syndrome with mild mental retardation and with growth retardationC Stoll, Y AlembikGenetic Counseling (Geneva, Switzerland)|January 22, 2005
Brachydactyly type E in two sibs with increased bone density and mental retardation. A new autosomal recessive syndrome?C Stoll, Y AlembikGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Oto-palato-digital syndrome type IIC Stoll, Y AlembikGenetic Counseling (Geneva, Switzerland)|January 1, 1994
A boy with neurofibromatosis 1 and Poland anomalyY Alembik, C StollAnnales De Genetique|May 26, 1998
Impact of routine fetal ultrasonographic screening on the prevalence of Down syndrome in non aged mothersC Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Complex congenital heart disease, microcephaly, pheochromocytoma and neurofibromatosis type I in a girl born from consanguineous parentsC Stoll, Y Alembik, B DottAnnales De Genetique|January 1, 1994
Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?C Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Rett-like syndrome in fragile X syndromeY Alembik, B Dott, C StollAnnales De Genetique|December 9, 2003
Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrolC Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|January 1, 1994
A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parentsC Stoll, Y Alembik, P LutzPageof 29