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Genetic Counseling (Geneva, Switzerland)|February 26, 2013
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.Genetic Counseling (Geneva, Switzerland)|February 26, 2009
An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiologyP Prontera, F Escande, G Cocchi, et al.Genetic Counseling (Geneva, Switzerland)|December 18, 2013
Syndrome of inappropriate antidiuretic hormone secretion refractory to treatment in a newborn with alobar holoprosencephalyM N Cizmeci, M K Kanburoglu, A Z Akelma, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profileL De Smet, E Legius, G Fabry, et al.Genetic Counseling (Geneva, Switzerland)|May 3, 2001
A case of symbrachydactyly with oligodactylyM Seven, A Yuksel, A OzkilicGenetic Counseling (Geneva, Switzerland)|May 3, 2001
Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic featuresE Smeets, L Vandenbossche, J P FrynsGenetic Counseling (Geneva, Switzerland)|August 9, 2001
Prenatal diagnosis of familial hypercholesterolemia: importance of DNA analysis in the high-risk South African populationJ Vergotine, R Thiart, E Langenhoven, et al.Genetic Counseling (Geneva, Switzerland)|August 9, 2001
De novo ring chromosome 3 in a girl with hypoplastic thumb and coloboma of irisL O Barajas-Barajas, S Velarde-Félix, J Elizarrarás-Rivas, et al.Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Spondylothoracic dysostosis associated with diaphragmatic hernia and camptodactylyJ Swietliński, K Swist-Szulik, I Maruniak-Chudek, et al.Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Unilateral absent scaphoid in a patient with "Holt-Oram" syndromeL De SmetPageof 116