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Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Autosomal recessive congenital stenosis of aqueduct of SylviusP Barros-Nuñes, F RivasGenetic Counseling (Geneva, Switzerland)|January 1, 1993
An unclassifiable type of spondylo-peripheral epiphyseal dysplasia associated with 21 trisomyD M Ioan, M Popa, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome?C de Die-Smulders, H Vles, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Oculocerebrocutaneous syndrome: a case report, a follow-up, and differential diagnostic considerationsU Moog, G Krüger, B Stengel, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit geneA Sillén, C Wadelius, M Sundvall, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndromeA Verloes, S Lesenfants, B Philippet, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Ways of announcing a late-onset, heritable, disabling disease and their psychological consequencesC DelaporteGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the diseaseG Lucotte, N Gérard, P Roubertoux, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Mild phenotype in interstitial 4p deletion: another patient and review of the literatureG Van de Graaf, J M Sijstermans, J J Engelen, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Autosomal dominant congenital epiphyseal dysplasia limited to the femoral headsA Hernández, Z Nazara, M C Reynoso, et al.Pageof 116