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European Journal of Pediatrics|March 29, 2001
A characteristic EEG pattern in 4p-syndrome: case report and review of the literatureA Zankl, M C Addor, M M Maeder-Ingvar, et al.Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Two brothers with atypical syndactylies, cerebellar atrophy and severe mental retardationD F Schorderet, M C Addor, Ph Maeder, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new case of Pfeiffer syndrome with mutation in FGFR2M C Addor, F Gudinchet, R N Laurini, et al.European Journal of Pediatrics|June 5, 2001
Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA geneA Zankl, M C Addor, P Cousin, et al.Neuropediatrics|December 7, 2007
Atypical presentation of Prader-Willi syndrome with cerebral venous thrombosis: association or fortuity?L Beretta, M Hauschild, P-Y Jeannet, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1995
"C" trigonocephaly syndrome with diaphragmnatic herniaM C Addor, D Stefanutti, F Farron, et al.Ophthalmic Genetics|March 23, 2001
Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patientsR I Bojinova, D F Schorderet, M C Addor, et al.BJOG : an International Journal of Obstetrics and Gynaecology|February 6, 2014
Prevalence and risk of Down syndrome in monozygotic and dizygotic multiple pregnancies in Europe: implications for prenatal screeningB Boyle, J K Morris, R McConkey, et al.Revue D'Epidemiologie Et De Sante Publique|February 14, 2006
Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999H Dolk, M Loane, E Garne, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 25, 2004
Prenatal diagnosis of severe structural congenital malformations in EuropeE Garne, M Loane, H Dolk, et al.Pageof 3