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Results of search for 'au:"Lund, A M"', page 1 of 3
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Authors
Borgwardt, L
Brixen, K
Christensen, E
Christensen, M
Christophersen, B O
Dali, C I
Dixon, M A
Duno, M
Eiberg, H
Fogh, J
Folkestad, L
Hald, J D
Harsløf, T
Jensen, B L
Leonard, J V
Lund, A M
Olsen, K J
Schwartz, M
Skovby, F
Thuesen, A M
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Adolescent
Adult
Animals
Cells, Cultured
Child
Child, Preschool
Collagen
DNA Mutational Analysis
Female
Humans
Infant
Male
Mutation
Osteogenesis Imperfecta
Pedigree
Phenotype
deficiency
diagnosis
genetics
metabolism
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1.
[The Angelman syndrome. Does the phenotype depend on maternal inheritance?].
[electronic resource]
by
Lund, A M
Producer:
19910904
In:
Ugeskrift for laeger
vol. 153
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2.
Questions about a vegan diet should be included in differential diagnostics of neurologically abnormal infants with failure to thrive.
[electronic resource]
by
Lund, A M
Producer:
20200901
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 108
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3.
Optic gliomas in children with neurofibromatosis type 1.
[electronic resource]
by
Lund, A M
Skovby, F
Producer:
19920114
In:
European journal of pediatrics
vol. 150
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4.
[Effective economizing with automobile and radio for home care. Interview by Lars Peter Bergqvist].
[electronic resource]
by
Lund, A M
Djurhuus, J
Producer:
19890810
In:
Sygeplejersken
vol. 89
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5.
[Neurofibromatosis type 1 in children].
[electronic resource]
by
Lund, A M
Skovby, F
Producer:
19940922
In:
Ugeskrift for laeger
vol. 156
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6.
Osteogenesis imperfecta: clinical, cephalometric, and biochemical investigations of OI types I, III, and IV.
[electronic resource]
by
Jensen, B L
Lund, A M
Producer:
19971208
In:
Journal of craniofacial genetics and developmental biology
vol. 17
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7.
False positive fructose loading: a pitfall in the diagnosis of fructose-1,6-bisphosphatase deficiency.
[electronic resource]
by
Lund, A M
Leonard, J V
Producer:
20010215
In:
Journal of inherited metabolic disease
vol. 23
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8.
Feeding difficulties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
[electronic resource]
by
Lund, A M
Leonard, J V
Producer:
20011214
In:
Archives of disease in childhood
vol. 85
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9.
Variable clinical expression in a family with OI type IV due to deletion of three base pairs in COL1A1.
[electronic resource]
by
Lund, A M
Schwartz, M
Skovby, F
Producer:
19970325
In:
Clinical genetics
vol. 50
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10.
Anthropometry of patients with osteogenesis imperfecta.
[electronic resource]
by
Lund, A M
Müller, J
Skovby, F
Producer:
19991014
In:
Archives of disease in childhood
vol. 80
Online resources:
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11.
(G586V) substitutions in the alpha 1 and alpha 2 chains of collagen I: effect of alpha-chain stoichiometry on the phenotype of osteogenesis imperfecta?
[electronic resource]
by
Lund, A M
Skovby, F
Schwartz, M
Producer:
19970717
In:
Human mutation
vol. 9
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12.
Genetic counselling and prenatal diagnosis of osteogenesis imperfecta caused by paternal mosaicism.
[electronic resource]
by
Lund, A M
Schwartz, M
Skovby, F
Producer:
19970306
In:
Prenatal diagnosis
vol. 16
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13.
Deletion of a Gly-Pro-Pro repeat in the pro alpha2(I) chain of procollagen I in a family with dominant osteogenesis imperfecta type IV.
[electronic resource]
by
Lund, A M
Skovby, F
Schwartz, M
Producer:
19960920
In:
Human genetics
vol. 97
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14.
Serine for glycine substitutions in the C-terminal third of the alpha 1(I) chain of collagen I in five patients with nonlethal osteogenesis imperfecta.
[electronic resource]
by
Lund, A M
Skovby, F
Schwartz, M
Producer:
19970626
In:
Human mutation
vol. 9
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15.
[Child abuse and osteogenesis imperfecta. How do we distinguish?].
[electronic resource]
by
Lund, A M
Skovby, F
Knudsen, F U
Producer:
20000714
In:
Ugeskrift for laeger
vol. 162
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16.
[Shaken baby syndrome].
[electronic resource]
by
Lund, A M
Sandgren, G
Knudsen, F U
Producer:
19981201
In:
Ugeskrift for laeger
vol. 160
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17.
Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity.
[electronic resource]
by
Lund, A M
Eiberg, H
Rosenberg, T
Warburg, M
Producer:
19920416
In:
Clinical genetics
vol. 41
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18.
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36.
[electronic resource]
by
Eiberg, H
Lund, A M
Warburg, M
Rosenberg, T
Producer:
19950817
In:
Human genetics
vol. 96
Online resources:
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19.
Comparison of Methods for Isolation of Listeria from Raw Milk.
[electronic resource]
by
Lund, A M
Zottola, E A
Pusch, D J
Publication details:
Journal of food protection
Aug 1991
In:
Journal of food protection
vol. 54
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20.
Atraumatic loss of a kidney in a patient with alpha1-antitrypsin deficiency.
[electronic resource]
by
Randers, E
Jønler, M
Lund, A M
Danielsen, H
Producer:
19981030
In:
Nephron
vol. 80
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