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American Journal of Medical Genetics. Part A|May 19, 2009
Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganizationB Isidor, G Baujat, C Le Caignec, et al.American Journal of Human Genetics|May 22, 2002
Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1C Le Caignec, M Lefevre, J J Schott, et al.Clinical Genetics|June 24, 2010
Identification of two novel mutations in Shh long-range regulator associated with familial pre-axial polydactylyJ Albuisson, B Isidor, M Giraud, et al.Prenatal Diagnosis|February 8, 2003
Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetusC Le Caignec, M Boceno, M Joubert, et al.Human Mutation|April 19, 2006
Optimization and evaluation of single-cell whole-genome multiple displacement amplificationC Spits, C Le Caignec, M De Rycke, et al.Human Molecular Genetics|August 15, 2000
Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndromeN Bondurand, V Pingault, D E Goerich, et al.European Journal of Medical Genetics|January 2, 2014
Distinct phenotype of PHF6 deletions in femalesN Di Donato, B Isidor, S Lopez Cazaux, et al.American Journal of Medical Genetics. Part A|May 13, 2008
Autosomal dominant spondylocarpotarsal synostosis syndrome: phenotypic homogeneity and genetic heterogeneityB Isidor, V Cormier-Daire, M Le Merrer, et al.Journal of Medical Genetics|February 4, 2005
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformationsC Le Caignec, M Boceno, P Saugier-Veber, et al.American Journal of Medical Genetics. Part A|October 16, 2010
Tibial developmental field defect in valproic acid embryopathy: Report on three casesJ L Alessandri, B Isidor, A David, et al.Pageof 3