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American Journal of Medical Genetics|October 1, 1987
Prenatal detection of Salla disease based upon increased free sialic acid in amniocytesM Renlund, P AulaHuman Genetics|May 19, 1976
Distribution of spontaneous chromosome breaks in human chromosomesP Aula, H von KoskullHuman Genetics|May 1, 1995
A molecular and cytogenetic study in Finnish Prader-Willi patientsH Kokkonen, M Kähkönen, J LeistiThe Journal of Reproductive Medicine|May 1, 1987
Transient fetal ascites and hydrops with a favorable outcome. A report of two casesP Kirkinen, P Jouppila, J LeistiPrenatal Diagnosis|March 1, 1987
Early prenatal diagnosis of a lethal syndrome of multiple congenital contracturesP Kirkinen, R Herva, J LeistiEpilepsia|August 1, 1995
Northern epilepsy syndrome: clinical course and the effect of medication on seizuresA Hirvasniemi, P Herrala, J LeistiNeuropediatrics|December 1, 1994
Lethal arthrogryposis in Finland--a clinico-pathological study of 83 cases during thirteen yearsK Vuopala, J Leisti, R HervaHuman Genetics|May 1, 1991
Uridine enhances expression of the fragile X chromosome in human lymphocytesM Kähkönen, R Haataja, J LeistiJournal of Medical Genetics|January 1, 1996
Haplotype analysis in prenatal diagnosis and carrier identification of Salla diseaseJ Schleutker, P Sistonen, P AulaPediatric Research|June 1, 1976
Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samplesP Aula, K Raivio, S AutioPageof 17