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Results of search for 'au:"Jacobs, L J A M"'
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Authors
Galjaard, R J H
Geraedts, J P M
Jacobs, L J A M
Jongbloed, R J E
Los, F J
Niermeijer, M F
Nijland, J G
Scholte, H R
Schoonderwoerd, K
Smeets, H J M
Wijburg, F A
de Coo, I F M
de Klerk, J B C
de Wert, G
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Topics
Anemia
Animals
Bone Marrow Diseases
Cell Nucleus
Child
Child, Preschool
DNA Mutational Analysis
DNA, Mitochondrial
Dimerization
Disease Models, Animal
Fatal Outcome
Female
Fibrosis
Gene Deletion
Humans
Male
Phenotype
Pregnancy
Prenatal Diagnosis
genetics
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English
Your search returned 3 results.
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1.
The transmission of OXPHOS disease and methods to prevent this.
[electronic resource]
by
Jacobs, L J A M
de Wert, G
Geraedts, J P M
de Coo, I F M
Smeets, H J M
Producer:
20060405
In:
Human reproduction update
vol. 12
Online resources:
Available from publisher's website
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No items available.
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2.
Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation.
[electronic resource]
by
Jacobs, L J A M
de Coo, I F M
Nijland, J G
Galjaard, R J H
Los, F J
Schoonderwoerd, K
Niermeijer, M F
Geraedts, J P M
Scholte, H R
Smeets, H J M
Producer:
20051103
In:
Molecular human reproduction
vol. 11
Online resources:
Available from publisher's website
Availability:
No items available.
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3.
Pearson syndrome and the role of deletion dimers and duplications in the mtDNA.
[electronic resource]
by
Jacobs, L J A M
Jongbloed, R J E
Wijburg, F A
de Klerk, J B C
Geraedts, J P M
Nijland, J G
Scholte, H R
de Coo, I F M
Smeets, H J M
Producer:
20041012
In:
Journal of inherited metabolic disease
vol. 27
Online resources:
Available from publisher's website
Availability:
No items available.
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