Showing results (851-860 of 7,173) with videos related to
Sort By:
Pageof 718
Clinical Genetics|January 1, 1996
An improved method for the detection of Down's syndrome aneuploidy in uncultured amniocytesM Pierluigi, C Perfumo, S Cavani, et al.Clinical Genetics|January 1, 1996
Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delayC M Aalfs, M E Jacobs, M A Nieste-Otter, et al.Clinical Genetics|August 1, 1993
Effect of the fragile X anomaly on body proportions estimated by pedigree analysisD Z Loesch, M L SampsonClinical Genetics|September 1, 1993
Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22)F A Baumeister, J Egger, M T Schildhauer, et al.Clinical Genetics|September 1, 1993
Prenatal detection of an inverted X chromosome in a maleA R Brothman, A Newlin, S E Phillips, et al.Clinical Genetics|September 1, 1993
Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23J P Fryns, P Strømme, H van den BergheClinical Genetics|September 1, 1993
Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12F Speleman, N Van Roy, E De Vos, et al.Clinical Genetics|March 1, 1979
Regional mapping of the HLA on the short arm of chromosome 6R Berger, A Bernheim, M Sasportes, et al.Clinical Genetics|March 1, 1979
Prenatal diagnosis of polycystic kidneys and encephalocele (Meckel syndrome)U Friedrich, K B Hansen, M Hauge, et al.Clinical Genetics|November 4, 2004
Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasiaK Brusgaard, A D Kjeldsen, L Poulsen, et al.Pageof 718