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Results of search for 'au:"Van Beurden, E"', page 2 of 2
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Authors
Barnett, L
Barnett, L M
Beard, J
Berger, R
Brooks, L O
Christian, J
Dietrich, U C
Henrikson, D
James, R
Malingré, H E
Newman, B
Ottenhoff-Kalff, A E
Poll-The, B T
Rijksen, G
Tyler, C
Van Beurden, E
Zask, A
van Beurden, E
van Beurden, E A
van den Berg, I E
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Your search returned 25 results.
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21.
Functional interaction between the epidermal growth factor receptor and c-Src kinase activity.
[electronic resource]
by
Oude Weernink, P A
Ottenhoff-Kalff, A E
Vendrig, M P
van Beurden, E A
Staal, G E
Rijksen, G
Producer:
19941107
In:
FEBS letters
vol. 352
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22.
Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).
[electronic resource]
by
van den Berg, I E
van Beurden, E A
de Klerk, J B
van Diggelen, O P
Malingré, H E
Boer, M M
Berger, R
Producer:
19971022
In:
American journal of human genetics
vol. 61
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23.
X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.
[electronic resource]
by
van den Berg, I E
van Beurden, E A
Malingré, H E
van Amstel, H K
Poll-The, B T
Smeitink, J A
Lamers, W H
Berger, R
Producer:
19950309
In:
American journal of human genetics
vol. 56
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24.
Hereditary tyrosinemia type 1: novel missense, nonsense and splice consensus mutations in the human fumarylacetoacetate hydrolase gene; variability of the genotype-phenotype relationship.
[electronic resource]
by
Ploos van Amstel, J K
Bergman, A J
van Beurden, E A
Roijers, J F
Peelen, T
van den Berg, I E
Poll-The, B T
Kvittingen, E A
Berger, R
Producer:
19960223
In:
Human genetics
vol. 97
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25.
Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency--a neurometabolic disorder associated with reduced L-serine biosynthesis.
[electronic resource]
by
Klomp, L W
de Koning, T J
Malingré, H E
van Beurden, E A
Brink, M
Opdam, F L
Duran, M
Jaeken, J
Pineda, M
Van Maldergem, L
Poll-The, B T
van den Berg, I E
Berger, R
Producer:
20010118
In:
American journal of human genetics
vol. 67
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