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Clinical Genetics
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September 1, 1986
Frequency of rare fragile sites among mentally subnormal schoolchildren
M 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 parents
P Aula, V Näntö, M L Laipio, et al.
Monographs in Human Genetics
|
January 1, 1972
Biochemical and fine structural studies in aspartylglucosaminuria
J 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 syndrome
J 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 fibroblasts
E L Punnonen, S Autio, V S Marjomäki, et al.
Clinical Genetics
|
August 1, 1985
Partial trisomy 12q: clinical and cytogenetic observations
C Tengström, M Wilska, M Kähkönen, et al.
Lancet (London, England)
|
November 10, 1973
Letter: Mulibrey nanism v. hereditary congenital dwarfism with pericardial constriction
J Perheentupa, S Autio, S Leisti, et al.
Lancet (London, England)
|
August 18, 1973
Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction
J Perheentupa, S Autio, S Leisti, et al.
Acta Neurologica Scandinavica
|
May 1, 1993
Epileptic seizures in aspartylglucosaminuria: a common disorder
M Arvio, V Oksanen, S Autio, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 66) with videos related to
Sort By:
Page
of 7
Clinical Genetics
|
September 1, 1986
Frequency of rare fragile sites among mentally subnormal schoolchildren
M 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 parents
P Aula, V Näntö, M L Laipio, et al.
Monographs in Human Genetics
|
January 1, 1972
Biochemical and fine structural studies in aspartylglucosaminuria
J 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 syndrome
J 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 fibroblasts
E L Punnonen, S Autio, V S Marjomäki, et al.
Clinical Genetics
|
August 1, 1985
Partial trisomy 12q: clinical and cytogenetic observations
C Tengström, M Wilska, M Kähkönen, et al.
Lancet (London, England)
|
November 10, 1973
Letter: Mulibrey nanism v. hereditary congenital dwarfism with pericardial constriction
J Perheentupa, S Autio, S Leisti, et al.
Lancet (London, England)
|
August 18, 1973
Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction
J Perheentupa, S Autio, S Leisti, et al.
Acta Neurologica Scandinavica
|
May 1, 1993
Epileptic seizures in aspartylglucosaminuria: a common disorder
M Arvio, V Oksanen, S Autio, et al.
Page
of 7