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Submited on: 01 Nov 2011 12:31:07 PM GMT
Published on: 02 Nov 2011 05:42:47 PM GMT
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Other Comments:
the results and discussion are too short, I guess that they might be separated and widely discussed.
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Competing interests:
no
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Invited by the author to review this article? :
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Have you previously published on this or a similar topic?:
No
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References:
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Experience and credentials in the specific area of science:
genetics lead faculty
- How to cite: Lo Vasco V .A New PCR-RFLP Method for Diagnosing PNPLA3 rs738409 Polymorphism [Review of the article 'A New PCR-RFLP Method for Diagnosing PNPLA3 rs738409 Polymorphism ' by Dutta A].WebmedCentral 2011;2(11):WMCRW001090
The manuscript in its current form displays considerable limitations in content, and would basically require restructuring to make it a valuable contribution.
For instance, the result and discussion sections appear particularly weak. A more stringent description of the data will help to streamline this article: (The Figure 1 is not included???).
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Genetic and molecular diagnosis of fragile X syndrome