Author/Creator: Boustred, C. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Boustred, C.

1. A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly. Issue 4 (11th February 2018)

Authors:: Ishida, M.; Cullup, T.; Boustred, C.; James, C.; Docker, J.; English, C.; Lench, N.; Copp, A.J.; Moore, G.E.; Greene, N.D.E.; Stanier, P.
Journal:: Clinical genetics
Issue:: Volume 93:Issue 4(2018)
Page Start:: 870
Record Type:: Journal Article
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2. Sensitivity and specificity of biochemical screening for Familial Hypercholesterolaemia in childhood: Avon Longitudinal Study of Parents and Children (ALSPAC). (September 2017)

Authors:: Humphries, S.E.; Futema, M.; Cooper, J.A.; Charakida, M.; Boustred, C.; Sattar, N.; Deanfield, J.; Lawlor, D.A.; Timpson, N.J.; Hingorani, A.D.
Journal:: Atherosclerosis
Issue:: Volume 28(2017)
Page Start:: e5
Record Type:: Journal Article
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3. Would raising the total cholesterol diagnostic cut-off from 7.5 mmol/L to 9.3 mmol/L improve detection rate of patients with monogenic familial hypercholesterolaemia?. Issue 2 (April 2015)

Authors:: Futema, M.; Kumari, M.; Boustred, C.; Kivimaki, M.; Humphries, S.E.
Journal:: Atherosclerosis
Issue:: Volume 239:Issue 2(2015)
Page Start:: 295
Record Type:: Journal Article
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4. Would raising the total cholesterol diagnostic cut-off from 7.5 mmol/L to 9.3 mmol/L improve detection rate of patients with monogenic familial hypercholesterolaemia?. Issue 2 (April 2015)

Authors:: Futema, M.; Kumari, M.; Boustred, C.; Kivimaki, M.; Humphries, S.E.
Journal:: Atherosclerosis
Issue:: Volume 239:Issue 2(2015)
Page Start:: 295
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗