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American Journal of Medical Genetics. Part A|February 3, 2004
Two cousins with partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of the chromosome 12Clotilde Lagier-Tourenne, E Ginglinger, Y Alembik, et al.American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.Journal of Dental Research|November 26, 2008
Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a reviewF Clauss, M-C Manière, F Obry, et al.Prenatal Diagnosis|January 25, 2013
Postnatal phenotype according to prenatal ultrasound features of Noonan syndrome: a retrospective study of 28 casesA Gaudineau, B Doray, E Schaefer, et al.Neuroepidemiology|January 1, 1994
Gender distributions in parents and children concordant for multiple sclerosisM P Roth, J Clayton, E Patois, et al.Clinical Dysmorphology|October 26, 1999
Familial association of camptodactyly, mental retardation, whistling face and Pierre Robin sequenceC Stoll, F Benoit, M O Peter, et al.Zentralblatt Fur Neurochirurgie|June 5, 1999
[Keratocysts of the jaws with an expansion to the skull base]F Soost, C Stoll, O Gerhardt, et al.Journal of Medical Genetics|May 1, 1993
Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardationC Stoll, D Chognot, A Halb, et al.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.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.Pageof 33