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- 2000
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Mark
CDG type 1B : Kliniek, diagnostiek en behandeling
(
- Contribution to journal › Article
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Mark
Mevalonic aciduria in 12 unrelated patients with hygerimmunoglobulinaemia D and periodic fever syndrome
(
- Contribution to journal › Article
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Mark
Congenital hepatic fibrosis in 3 siblings with phosphomannose isomerase deficiency
(
- Contribution to journal › Article
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Mark
Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency - A neurometabolic disorder associated with reduced L-serine biosynthesis
(
- Contribution to journal › Article
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Mark
Atrial septal defect in adults. Thirty-eight-year follow-up of a surgically and a conservatively managed group
(
- Contribution to journal › Article
- 1999
-
Mark
Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli's disease)
(
- Contribution to journal › Article
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Mark
[A trauma course for medical students prepares physicians for emergency service]
(
- Contribution to journal › Article
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Mark
Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas
(
- Contribution to journal › Article
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Mark
Cytogenetic analyses of secondary liver tumors reveal significant differences in genomic imbalances between primary and metastatic colon carcinomas
(
- Contribution to journal › Article
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Mark
Sertoli cells decrease microglial response and increase engraftment of human hNT neurons in the hemiparkinsonian rat striatum
(
- Contribution to journal › Article