Indian Journal of Human Genetics
Home Current Issue Archives Guidelines Subscriptions e-Alerts Login
Users online: 36
Print this page  Email this page Small font sizeDefault font sizeIncrease font size
Export selected to
Endnote
Reference Manager
Procite
Medlars Format
RefWorks Format
BibTex Format
   Table of Contents
Coverpage
May-August 2011
Volume 17 | Issue 2
Page Nos. 43-113

Online since Monday, October 17, 2011

Accessed 43,878 times.

PDF access policy
Full text access is free in HTML pages; however the journal allows PDF access only to users from INDIA and paid subscribers.

EPub access policy
Full text in EPub is free except for the current issue. Access to the latest issue is reserved only for the paid subscribers.
View as eBookView issue as eBook
Author Institution MappingAuthor Institution Mapping
CitationsIssue citations
Access StatisticsIssue statistics
RSS FeedRSS
Show all abstracts  Show selected abstracts  Export selected to  Add to my list
EDITORIALS  

Chromosomal aberrations in hematological malignancies: A guide to the identification of novel oncogenes p. 43
Babu Rao Vundinti, Kanjaksha Ghosh
DOI:10.4103/0971-6866.86168  PMID:22090710
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta

Are mannose-binding lectin gene 2 (MBL2) polymorphisms and MBL deficiency associated with infections? p. 45
Vandana Pradhan, Ajit Gorakshakar
DOI:10.4103/0971-6866.86170  PMID:22090711
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta
REVIEW ARTICLE Top

Craniosynostosis genetics: The mystery unfolds Highly accessed article p. 48
Inusha Panigrahi
DOI:10.4103/0971-6866.86171  PMID:22090712
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (3) ]  [PubMed]  [Sword Plugin for Repository]Beta
ORIGINAL ARTICLES Top

Characterization of cryptic rearrangements, deletion, complex variants of PML, RARA in acute promyelocytic leukemia p. 54
Pratibha Kadam Amare, Chanda Baisane, Reena Nair, Hari Menon, Shripad Banavali, Sharayu Kabre, Sumit Gujral, P Subramaniam
DOI:10.4103/0971-6866.86174  PMID:22090713
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (2) ]  [PubMed]  [Sword Plugin for Repository]Beta

The first report described as an important study: The association of mannose-binding lectin gene 2 polymorphisms in children with down syndrome p. 59
Osman Demirhan, Deniz Tastemir, Ramazan Günesacar, Ali Irfan Güzel, Davut Alptekin
DOI:10.4103/0971-6866.86176  PMID:22090714
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (1) ]  [PubMed]  [Sword Plugin for Repository]Beta

Molecular investigation of mental retardation locus gene PRSS12 by linkage analysis p. 65
Zafar Ali, Masroor Ellahi Babar, Jamil Ahmad, Muhammad Zubair Yousaf, Muhammad Asif, Sajjad Ali Shah
DOI:10.4103/0971-6866.86178  PMID:22090715
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta

Novel mutations in arrhythmogenic right ventricular cardiomyopathy from Indian population p. 70
Pranathi Rao Pamuru, D V.N Maithili, Khalid Mohiuddin, Narasimhan Calambur, Pratibha Nallari
DOI:10.4103/0971-6866.86182  PMID:22090716
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (4) ]  [PubMed]  [Sword Plugin for Repository]Beta

Cytoprotective effect of honey against chromosomal breakage in fanconi anemia patients in vitro p. 77
Faeza Abdel Mogib El-Dahtory, Sohier Yahia
DOI:10.4103/0971-6866.86184  PMID:22090717
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (1) ]  [PubMed]  [Sword Plugin for Repository]Beta

Chromosomal abnormalities as a cause of recurrent abortions in Egypt p. 82
Faeza Abdel Mogib El-Dahtory
DOI:10.4103/0971-6866.86186  PMID:22090718
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (1) ]  [PubMed]  [Sword Plugin for Repository]Beta
BRIEF REPORTS Top

Association of cytotoxic T lymphocyte-associated antigen 4 gene single nucleotide polymorphism with type 1 diabetes mellitus in Madurai population of Southern India p. 85
Beatrice Philip, W Isabel
DOI:10.4103/0971-6866.86189  PMID:22090719
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (7) ]  [PubMed]  [Sword Plugin for Repository]Beta

G-C heterozygosis in mutS homolog2 as a risk factor to hereditary nonpolyposis colon cancer in the absence of a family medical history p. 90
Jorge Alfonso Arvayo-Zatarain, José Manuel Grijalva-Chon, Reina Castro-Longoria, Alejandro Varela-Romero
DOI:10.4103/0971-6866.86191  PMID:22090720
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta
CASE REPORTS Top

McKusick-Kaufman or Bardet-Biedl syndrome? A new borderline case in an Italian nonconsanguineous healthy family p. 94
Massimiliano Chetta, Nenad Bukvic, Valeria Bafunno, Michelina Sarno, Rosario Magaldi, Gianpaolo Grilli, Vincenzo Bertozzi, Francesco Perfetto, Maurizio Margaglione
DOI:10.4103/0971-6866.86194  PMID:22090721
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (1) ]  [PubMed]  [Sword Plugin for Repository]Beta

A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review p. 97
Siham Chafai Elalaoui, Tajir Mariam, Ratbi Ilham, Doubaj Yassamine, Sefiani Abdelaziz
DOI:10.4103/0971-6866.86197  PMID:22090722
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta

Deletion of ABL/BCR on der(9) associated with severe basophilia p. 100
Shantashri Vaidya, Manisha Madkaikar, Kanjaksha Ghosh, Babu Rao Vundinti
DOI:10.4103/0971-6866.86198  PMID:22090723
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta

Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met) p. 104
Zoran Gucev, Nevenka Slavevska, Velibor Tasic, Nevenka Laban, Nada Pop-Jordanova, Dragan Danilovski, Jacqueline Woolf, Duncan Cole
DOI:10.4103/0971-6866.86199  PMID:22090724
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [PubMed]  [Sword Plugin for Repository]Beta

Early recurrent left atrial myxoma in a teenager with de novo mutation of Carney complex p. 108
Mila S Stajevic, Vladislav A Vukomanovic, Vladimir D Kuburovic, Slavisa M Djuricic
DOI:10.4103/0971-6866.86200  PMID:22090725
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (3) ]  [PubMed]  [Sword Plugin for Repository]Beta

Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18 p. 111
Eiman Bagherizadeh, Farkhondeh Behjati, Seyed Hoseinali Saberi, Yousef Shafeghati
DOI:10.4103/0971-6866.86201  PMID:22090726
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Citations (2) ]  [PubMed]  [Sword Plugin for Repository]Beta
  Search 
  The Journal 
  The Association 
  Site Statistics 
  Addresses 
  My Preferences 
  Online Submission 
  Next Issue
  Previous Issue

Submit Articles

Alerts

Join us