Showing results (71-80 of 899) with videos related to
Sort By:
Pageof 90
Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, et al.Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.Prenatal Diagnosis|May 10, 2002
Prenatal findings in a monozygotic twin pregnancy with Costello syndromeT Van den Bosch, D Van Schoubroeck, J P Fryns, et al.Genomics|December 1, 1996
Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, P Debeer, et al.Annales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.Clinical Genetics|December 17, 2009
DISC1 duplication in two brothers with autism and mild mental retardationA Crepel, J Breckpot, J-P Fryns, 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.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.Advances in Dental Research|January 23, 2018
Erythritol Functional Roles in Oral-Systemic HealthP de CockPageof 90