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Works by Vincent JB

Results: 6

1

Identification of genomic deletions spanning the PCDH19 gene in two unrelated girls with intellectual disability and seizures.

Published in:

Clinical Genetics, 2012, v. 82, n. 6, p. 540, doi. 10.1111/j.1399-0004.2011.01812.x

By:

Vincent, AK;
Noor, A;
Janson, A;
Minassian, BA;
Ayub, M;
Vincent, JB;
Morel, CF

Publication type:

Article

2

Quest for the molecular mechanism of chromium action and its relationship to diabetes.

Published in:

2000

By:

Vincent JB

Publication type:

Journal Article

3

Recent advances in the nutritional biochemistry of trivalent chromium.

Published in:

2004

By:

Vincent JB

Publication type:

Journal Article

4

Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome.

Published in:

Human Mutation, 1998, v. 12, n. 6, p. 431, doi. 10.1002/(SICI)1098-1004(1998)12:6<431::AID-HUMU10>3.0.CO;2-Y

By:

Vincent, JB;
Gurling, Hugh M. D.

Publication type:

Article

5

Comment on: Padmavathi et al. (2010) Chronic Maternal Dietary Chromium Restriction Modulates Visceral Adiposity: Probable Underlying Mechanisms. Diabetes;59:98-104.

Published in:

2010

By:

Vincent JB;
Rasco JF

Publication type:

Journal Article

6

Association of alpha 4Beta 2 nicotinic receptor and heavy smoking in schizophrenia.

Published in:

2007

By:

Voineskos S;
De Luca V;
Mensah A;
Vincent JB;
Potapova N;
Kennedy JL

Publication type:

Journal Article