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Indian Journal of Human Genetics (IJHG)

Publisher :

Medknow Publications

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Peer reviewed only
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Open Access
  • Human Genetics
  • Genetics
  • Medical

    • +5

e-ISSN :

0971-6866

Issue Frequency :

Monthly

Est. Year :

2013

Mobile :

2266491818

DOI :

YES

Country :

India

Language :

British English

APC :

YES

Impact Factor Assignee :

Google Scholar

Email :

ijhg_iih@yahoo.co.in

Journal Descriptions

Include Summary of key findings (primary outcome measures, secondary outcome measures, results as they relate to a prior hypothesis); Strengths and limitations of the study (study question, study design, data collection, analysis and interpretation); Interpretation and implications in the context of the totality of evidence (is there a systematic review to refer to, if not, could one be reasonably done here and now?, what this study adds to the available evidence, effects on patient care and health policy, possible mechanisms); Controversies raised by this study; and Future research directions (for this particular research collaboration, underlying mechanisms, clinical research). Do not repeat in detail data or other material given in the Introduction or the Results section.


Indian Journal of Human Genetics (IJHG) is :

International, Peer-Reviewed, Open Access, Refereed, Human Genetics, Genetics, Medical, Health, Health Science and technology, Human genetics Periodicals, Medical genetics, Science and technology , Online Monthly Journal

UGC Approved, ISSN Approved: P-ISSN , E-ISSN - 0971-6866, Established in - 2013, Impact Factor

Provide Crossref DOI

Indexed in Scopus, PubMed

Not indexed in WoS, DOAJ, UGC CARE

Indexing

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PubMed
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+3 More

Publications of IJHG

  • dott image March, 2013

Distribution of CC-chemokine receptor-5-Δ32 allele among the tribal and caste population of Vidarbha region of Maharashtra state

Genetic relationships among the ethnic groups are not uniform across the geographical region. Considering this assumption, we analyzed the frequency of the CC-chemokine receptor-5 (CCR5)-∆...

  • dott image January, 2013

Prevalence of MTHFR 677 C-T polymorphism among mothers of Down syndrome children.

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