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Results of search for 'au:"Langenhoven, E"', page 1 of 2
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Authors
Coetzee, G A
Grobbelaar, J J
Kotze, M J
Kriek, J A
Langenhoven, E
Loubser, O
Marais, A D
Marx, M P
Oosthuizen, C J
Peeters, A V
Retief, A E
Rubinsztein, D C
Steyn, K
Theart, L
Thiart, R
Van Gaal, L F
Warnich, L
Weich, H F
du Plessis, L
van der Westhuyzen, D R
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Topics
Adolescent
Adult
Base Sequence
Child
DNA
Female
Humans
Hyperlipoproteinemia Type II
Male
Middle Aged
Molecular Sequence Data
Mutation
Pedigree
Polymerase Chain Reaction
Polymorphism, Genetic
Receptors, LDL
South Africa
blood
ethnology
genetics
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English
Your search returned 27 results.
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1.
Improved visualization of the Bst EII RFLP of the human LDL receptor gene by co-digestion.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Retief, A E
Producer:
19880223
In:
Nucleic acids research
vol. 15
Online resources:
Available from publisher's website
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2.
A de novo duplication in the low density lipoprotein receptor gene.
[electronic resource]
by
Kotze, M J
Theart, L
Peeters, A
Langenhoven, E
Producer:
19951214
In:
Human mutation
vol. 6
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3.
A RFLP associated with the low-density lipoprotein receptor gene (LDLR).
[electronic resource]
by
Kotze, M J
Langenhoven, E
Dietzsch, E
Retief, A E
Producer:
19870410
In:
Nucleic acids research
vol. 15
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4.
Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene.
[electronic resource]
by
Warnich, L
Kotze, M J
Langenhoven, E
Retief, A E
Producer:
19920716
In:
Human genetics
vol. 89
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5.
Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Peeters, A V
Theart, L
Oosthuizen, C J
Producer:
19950503
In:
Molecular and cellular probes
vol. 8
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6.
An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics.
[electronic resource]
by
Kotze, M J
Warnich, L
Langenhoven, E
du Plessis, L
Retief, A E
Producer:
19900717
In:
Journal of medical genetics
vol. 27
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7.
The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Warnich, L
du Plessis, L
Retief, A E
Producer:
19911206
In:
Annals of human genetics
vol. 55
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8.
Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor gene.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Warnich, L
Marx, M P
Retief, A E
Producer:
19891115
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 76
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9.
Report on a molecular diagnostic service for familial hypercholesterolemia in Afrikaners.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Theart, L
Marx, M P
Oosthuizen, C J
Producer:
19940812
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
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10.
Two novel frameshift mutations in the low density lipoprotein receptor gene generated by endogenous sequence-directed mechanisms.
[electronic resource]
by
Peeters, A V
Van Gaal, L F
Theart, L
Langenhoven, E
Kotze, M J
Producer:
19951120
In:
Human genetics
vol. 96
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11.
DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Kriek, J A
Oosthuizen, C J
Retief, A E
Producer:
19921008
In:
Clinical genetics
vol. 42
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12.
Recurrent LDL-receptor mutation causes familial hypercholesterolaemia in South African coloureds and Afrikaners.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Theart, L
Loubser, O
Micklem, A
Oosthuizen, C J
Producer:
19950908
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 85
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13.
Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations.
[electronic resource]
by
Kotze, M J
Theart, L
Callis, M
Peeters, A V
Thiart, R
Langenhoven, E
Producer:
19951207
In:
PCR methods and applications
vol. 4
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14.
Prenatal diagnosis of familial hypercholesterolemia: importance of DNA analysis in the high-risk South African population.
[electronic resource]
by
Vergotine, J
Thiart, R
Langenhoven, E
Hillermann, R
De Jong, G
Kotze, M J
Producer:
20020128
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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15.
Intrafamilial variability in the clinical expression of familial hypercholesterolemia: importance of risk factor determination for genetic counselling.
[electronic resource]
by
Kotze, M J
Davis, H J
Bissbort, S
Langenhoven, E
Brusnicky, J
Oosthuizen, C J
Producer:
19931014
In:
Clinical genetics
vol. 43
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16.
Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics.
[electronic resource]
by
Kotze, M J
Peeters, A V
Langenhoven, E
Wauters, J G
Van Gaal, L F
Producer:
19950512
In:
Atherosclerosis
vol. 111
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17.
Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.
[electronic resource]
by
Kotze, M J
Langenhoven, E
Retief, A E
Seftel, H C
Henderson, H E
Weich, H F
Producer:
19890622
In:
Journal of medical genetics
vol. 26
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18.
Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and Indians.
[electronic resource]
by
Rubinsztein, D C
Coetzee, G A
van der Westhuyzen, D R
Langenhoven, E
Kotze, M J
Producer:
19950908
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 85
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19.
Screening for mutations in exon 4 of the LDL receptor gene: identification of a new deletion mutation.
[electronic resource]
by
Theart, L
Kotze, M J
Langenhoven, E
Loubser, O
Peeters, A V
Lintott, C J
Scott, R S
Producer:
19950823
In:
Journal of medical genetics
vol. 32
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20.
High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa.
[electronic resource]
by
de Villiers, J N
Hillerman, R
de Jong, G
Langenhoven, E
Rossouw, H
Marx, M P
Kotze, M J
Producer:
19990603
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 89
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