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Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Proteus syndrome: a case with clonal chromosome aberrationD Gieruszczak-Bialek, M Illiszko, W Mikolajczyk, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Partial trisomy 20q in a newborn with dextrocardiaM C Addor, C Castagne, J L Micheli, et al.
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisationM Alkan, G P Ramelli, H Hirsiger, et al.
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescenceT Lukusa, J P Fryns
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Lenz microphthalmia syndrome: three additional cases with rare associated anomaliesS A Temtamy, S I Ismail, N A Meguid
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Osteopathia striata with cranial sclerosis: literature reappraisal argues for X-linked inheritanceC Behninger, H D Rott
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Wolf-Hirschhorn (4p-)syndrome in a near adult with major depression; successful treatment with citalopramW M A Verhoeven, U Moog, A M A Wagemans, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literatureP Franceschini, D Licata, A Guala, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?D M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.
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