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Human Genetics|September 1, 1987
Prevalence of the fragile X syndrome in four birth cohorts of children of school ageM Kähkönen, T Alitalo, E Airaksinen, 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.European Journal of Human Genetics : EJHG|June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the SaamiP Lahermo, M L Savontaus, P Sistonen, et al.Human Genetics|September 1, 1995
Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy numberM Laan, K Grön-Virta, A Salo, et al.Prenatal Diagnosis|March 1, 1984
Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in fetal developmental disordersM Heikinheimo, H Jalanko, J Leisti, et al.Archives of Disease in Childhood|August 1, 1992
Reversible mitochondrial myopathy with cytochrome c oxidase deficiencyM K Salo, J Rapola, H Somer, et al.Gene Therapy|February 4, 1999
Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouseM Peltola, A Kyttälä, O Heinonen, et al.Acta Neuropathologica|May 30, 1998
Atypical juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposit-like inclusions in the autonomic nerve cells of the gut wallL Aberg, I Järvelä, J Rapola, et al.Brain & Development|January 1, 1989
Muscle-eye-brain disease (MEB)P Santavuori, H Somer, K Sainio, et al.Pageof 27