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S Autio

Showing results (41-50 of 66) with videos related to

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Clinical Genetics|September 1, 1986
Frequency of rare fragile sites among mentally subnormal schoolchildrenM Kähkönen, J Leisti, C J Thoden, et al.
Clinical Genetics|January 1, 1973
Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parentsP Aula, V Näntö, M L Laipio, et al.
Monographs in Human Genetics|January 1, 1972
Biochemical and fine structural studies in aspartylglucosaminuriaJ Palo, P Riekkinen, A U Arstila, et al.
Birth Defects Original Article Series|January 1, 1975
Mulibrey nanism: review of 23 cases of a new autosomal recessive syndromeJ Perheentupa, S Autio, S Leisti, et al.
The Journal of Pediatrics|August 1, 1975
Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II)P Aula, J Rapola, S Autio, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 1, 1992
Autophagy, cathepsin L transport, and acidification in cultured rat fibroblastsE L Punnonen, S Autio, V S Marjomäki, et al.
Clinical Genetics|August 1, 1985
Partial trisomy 12q: clinical and cytogenetic observationsC Tengström, M Wilska, M Kähkönen, et al.
Lancet (London, England)|November 10, 1973
Letter: Mulibrey nanism v. hereditary congenital dwarfism with pericardial constrictionJ Perheentupa, S Autio, S Leisti, et al.
Lancet (London, England)|August 18, 1973
Mulibrey nanism, an autosomal recessive syndrome with pericardial constrictionJ Perheentupa, S Autio, S Leisti, et al.
Acta Neurologica Scandinavica|May 1, 1993
Epileptic seizures in aspartylglucosaminuria: a common disorderM Arvio, V Oksanen, S Autio, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Clinical Genetics|September 1, 1986
Frequency of rare fragile sites among mentally subnormal schoolchildrenM Kähkönen, J Leisti, C J Thoden, et al.
Clinical Genetics|January 1, 1973
Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parentsP Aula, V Näntö, M L Laipio, et al.
Monographs in Human Genetics|January 1, 1972
Biochemical and fine structural studies in aspartylglucosaminuriaJ Palo, P Riekkinen, A U Arstila, et al.
Birth Defects Original Article Series|January 1, 1975
Mulibrey nanism: review of 23 cases of a new autosomal recessive syndromeJ Perheentupa, S Autio, S Leisti, et al.
The Journal of Pediatrics|August 1, 1975
Prenatal diagnosis and fetal pathology of I-cell disease (mucolipidosis type II)P Aula, J Rapola, S Autio, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 1, 1992
Autophagy, cathepsin L transport, and acidification in cultured rat fibroblastsE L Punnonen, S Autio, V S Marjomäki, et al.
Clinical Genetics|August 1, 1985
Partial trisomy 12q: clinical and cytogenetic observationsC Tengström, M Wilska, M Kähkönen, et al.
Lancet (London, England)|November 10, 1973
Letter: Mulibrey nanism v. hereditary congenital dwarfism with pericardial constrictionJ Perheentupa, S Autio, S Leisti, et al.
Lancet (London, England)|August 18, 1973
Mulibrey nanism, an autosomal recessive syndrome with pericardial constrictionJ Perheentupa, S Autio, S Leisti, et al.
Acta Neurologica Scandinavica|May 1, 1993
Epileptic seizures in aspartylglucosaminuria: a common disorderM Arvio, V Oksanen, S Autio, et al.
Pageof 7