Showing results (111-120 of 161) with videos related to
Sort By:
Pageof 17
Birth Defects Original Article Series|January 1, 1974
The phenotype of human triploidyJ T Leisti, K O Raivio, M H Rapola, et al.Clinical Genetics|January 10, 2001
A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuriaO Järvinen, M Hietala, A M Aalto, et al.American Journal of Human Genetics|June 1, 1996
The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNAP Lahermo, A Sajantila, P Sistonen, et al.American Journal of Human Genetics|October 1, 1995
Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15J Schleutker, P Leppänen, J E Månsson, et al.Cancer Genetics and Cytogenetics|August 5, 1999
Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2P Huusko, K Castrén, V Launonen, et al.Human Genetics|September 1, 1997
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritanceK Silander, P Meretoja, H Pihko, et al.Genomics|March 1, 1992
Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in FinlandA C Syvänen, E Ikonen, T Manninen, et al.Infectious Diseases of Poverty|August 7, 2023
Optimisation of the DNA dipstick as a rapid extraction method for Schistosoma japonicum in infected mice samples and spiked human clinical samplesOyime P Aula, Donald P McManus, Malcolm K Jones, et al.British Medical Journal|November 29, 1980
Glial origin of rapidly adhering amniotic fluid cellsP Aula, H von Koskull, K Teramo, et al.Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.Pageof 17