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Genetic Counseling (Geneva, Switzerland)|January 1, 1995
A genetic diagnostic survey in an institutionalized population of 116 moderately to severely retarded male patients: the Rekem experienceC Schaap, C T Schrander-Stumpel, E T Colla-Pijkels, et al.Journal of Intellectual Disability Research : JIDR|February 20, 2002
Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrumM J Descheemaeker, A Vogels, V Govers, et al.American Journal of Medical Genetics|December 15, 1991
Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?A Spaepen, C Schrander-Stumpel, J P Fryns, et al.American Journal of Medical Genetics|May 1, 1988
Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy cultureM J McKinley, L U Kearney, K H Nicolaides, et al.Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.Clinical Genetics|December 1, 1985
Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1----p22)J P Fryns, A Kleczkowska, A M Dereymaker, et al.American Journal of Medical Genetics|February 22, 2002
Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler typeI Witters, Ph Moerman, K Devriendt, et al.European Journal of Medical Genetics|June 5, 2012
Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variantsM Isrie, G Froyen, K Devriendt, et al.American Journal of Medical Genetics|May 22, 1995
Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional familiesC Schrander-Stumpel, C Höweler, M Jones, et al.European Journal of Pediatrics|May 14, 1998
Vesico-ureteral reflux: a genetic condition?K Devriendt, P Groenen, H Van Esch, et al.Pageof 89