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   2012| May-August  | Volume 18 | Issue 2  
    Online since September 8, 2012

 
 
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CASE REPORTS
46,XX, der(15),t(Y;15)(q12;p11) karyotype in an azoospermic male
Serap T Onrat, Zafer Söylemez, Muhsin Elmas
May-August 2012, 18(2):241-245
DOI:10.4103/0971-6866.100785  PMID:23162305
  6,141 44 -
ORIGINAL ARTICLES
Rubinstein-taybi syndrome: Clinical profile of 11 patients and review of literature
Suresh Kumar, Renu Suthar, Inusha Panigrahi, Ram K Marwaha
May-August 2012, 18(2):161-166
DOI:10.4103/0971-6866.100751  PMID:23162289
  4,197 60 4
REVIEW ARTICLES
Stem cells: A potential regenerative future in dentistry
Sumit Narang, Nidhi Sehgal
May-August 2012, 18(2):150-154
DOI:10.4103/0971-6866.100749  PMID:23162287
  4,011 220 -
CASE REPORTS
Association of generalized aggressive periodontitis and ectrodactyly-ectodermal dysplasia-cleft syndrome
Rosamma Joseph, Sameera G Nath
May-August 2012, 18(2):259-262
DOI:10.4103/0971-6866.100793  PMID:23162310
  3,704 41 -
Mosaic triple X syndrome in a female with primary amenorrhea
A Venkateshwari, K Srimanjari, A Srilekha, Ashrafunnisa Begum, M Sujatha, T Sunitha, Pratibha Nallari, A Jyothy
May-August 2012, 18(2):246-249
DOI:10.4103/0971-6866.100790  PMID:23162306
  3,458 49 -
Genetic counseling in carriers of reciprocal translocations involving two autosomes
Bahareh Pourjafari, Hamid Pour-Jafari, Marzieh Farimani, Safieh Ghahramani, Ebrahim Kamrani Saleh
May-August 2012, 18(2):250-253
DOI:10.4103/0971-6866.100802  PMID:23162307
  3,290 50 -
Unusual manifestation of Marden-walker syndrome
Amar M Taksande, KY Vilhekar
May-August 2012, 18(2):256-258
DOI:10.4103/0971-6866.100798  PMID:23162309
  3,192 25 1
Smith-Lemli-Opitz-syndrome
Rachana Gedam, Ira Shah, Uma Ali, Alpana Ohri
May-August 2012, 18(2):235-237
DOI:10.4103/0971-6866.100779  PMID:23162303
  2,901 36 -
REVIEW ARTICLES
Toll-like receptors in autoimmunity with special reference to systemic lupus erythematosus
Vandana D Pradhan, Swaptagni Das, Prathamesh Surve, Kanjaksha Ghosh
May-August 2012, 18(2):155-160
DOI:10.4103/0971-6866.100750  PMID:23162288
  2,762 63 1
EDITORIALS
Neural tube defects: A need for population-based prevention program
Shubha Phadke, Meenal Agarwal
May-August 2012, 18(2):145-147
DOI:10.4103/0971-6866.100747  PMID:23162285
  2,672 138 1
ORIGINAL ARTICLES
Cytogenetic abnormalities in 222 infertile men with azoospermia and oligospermia in Iran: Report and review
Mohammad T Akbari, F Behjati, GR Pourmand, F Akbari Asbagh, M Ataei Kachoui
May-August 2012, 18(2):198-203
DOI:10.4103/0971-6866.100764  PMID:23162296
  2,708 85 2
CASE REPORTS
A case of Kartagener's syndrome: Importance of early diagnosis and treatment
Sanjay Gupta, Kumud K Handa, Ravi R Kasliwal, Pankaj Bajpai
May-August 2012, 18(2):263-267
DOI:10.4103/0971-6866.100787  PMID:23162311
  2,589 43 1
A familial deletion 4q syndrome: An outcome of a paracentric inversion
Meena Lall, Ratna Puri, Pushpa Saviour, Ishwar Verma
May-August 2012, 18(2):238-240
DOI:10.4103/0971-6866.100780  PMID:23162304
  2,515 32 -
ORIGINAL ARTICLES
Discerning non-disjunction in down syndrome patients by means of GluK1-(AGAT) n and D21S2055-(GATA) n microsatellites on chromosome 21
Ghosh Debarati, Sinha Swagata, Chatterjee Anindita, Nandagopal Krishnadas
May-August 2012, 18(2):204-216
DOI:10.4103/0971-6866.100769  PMID:23162297
  2,462 38 1
Prevalence and hematological profile of β-thalassemia and sickle cell anemia in four communities of Surat city
Dipal S Bhukhanvala, Smita M Sorathiya, Avani P Shah, Ankur G Patel, Snehalata C Gupte
May-August 2012, 18(2):167-171
DOI:10.4103/0971-6866.100752  PMID:23162290
  2,310 123 4
Genetic and environmental determinants of menstrual characteristics
Shayesteh Jahanfar
May-August 2012, 18(2):187-192
DOI:10.4103/0971-6866.100759  PMID:23162294
  2,208 42 3
EDITORIALS
Micro mapping the frequencies of beta thalassemia and sickle cell anemia in India: A way forward to plan control strategies
Reena Das
May-August 2012, 18(2):148-149
DOI:10.4103/0971-6866.100748  PMID:23162286
  2,055 132 2
ORIGINAL ARTICLES
Chromosomal abnormalities and hormonal disorders of primary amenorrhea patients in Egypt
Faeza El-Dahtory
May-August 2012, 18(2):183-186
DOI:10.4103/0971-6866.100758  PMID:23162293
  2,114 72 -
CASE REPORTS
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation
Karippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
May-August 2012, 18(2):233-234
DOI:10.4103/0971-6866.100776  PMID:23162302
  2,118 43 2
ORIGINAL ARTICLES
Molecular epidemiology of β-thalassemia in Pakistan: Far reaching implications
Saqib H Ansari, Tahir S Shamsi, Mushtaq Ashraf, Tasneem Farzana, Muneera Bohray, Kousar Perveen, Sajida Erum, Iqra Ansari, Muhammad Nadeem Ahmed, Masood Ahmed, Faizan Raza
May-August 2012, 18(2):193-197
DOI:10.4103/0971-6866.100762  PMID:23162295
  2,068 44 2
The study of gene GJB2/DFNB1 causing deafness in humans by linkage analysis from district Peshawar
Zafar Ali, Masroor Ellahi Babar, Jamil Ahmad, Sajjad Ali Shah
May-August 2012, 18(2):217-221
DOI:10.4103/0971-6866.100771  PMID:23162298
  1,815 27 -
Association of microsatellite instability and chronic obstructive pulmonary disorder in isocyanate-exposed population of Bhopal
Protiti Bose, Rashmi Bathri
May-August 2012, 18(2):172-176
DOI:10.4103/0971-6866.100754  PMID:23162291
  1,741 41 2
CASE REPORTS
Waardenburg syndrome: A rare genetic disorder, a report of two cases
Sudesh Kumar, Kiran Rao
May-August 2012, 18(2):254-255
DOI:10.4103/0971-6866.100804  PMID:23162308
  1,703 46 -
LETTERS TO THE EDITOR
An unusual clonal cytogenetic abnormality with t(15;17)(p11;q21) in a patient with severe aplastic anemia
Sanjeev K Sharma, Narendra Agrawal, Sonal Jain, Mohit Chowdhry, Pawan K Singh, Tulika Seth, Pravas Mishra, Manoranjan Mahapatra, Seema Tyagi, Haraprasad Pati
May-August 2012, 18(2):268-269
DOI:10.4103/0971-6866.100782  PMID:23162312
  1,550 36 -
ORIGINAL ARTICLES
Effect of maternal Tp53 gene G412C polymorphism on neural tube defects: A study from North India
Jyoti Arora, Kallur N Saraswathy, Roumi Deb
May-August 2012, 18(2):177-182
DOI:10.4103/0971-6866.100757  PMID:23162292
  1,529 44 -
BRIEF REPORT
An investigation of Ph 1 chromosome in chronic myeloid leukemia patients with different treatment modalities and hematological features
Koushik Chattopadhyay, Bibhas Kar
May-August 2012, 18(2):229-232
DOI:10.4103/0971-6866.100778  PMID:23162301
  1,532 38 -
ORIGINAL ARTICLES
Adjusted classification for ultrasound scoring index for antenatal detection of fetal trisomy
Viroj Wiwanitkit
May-August 2012, 18(2):226-228
DOI:10.4103/0971-6866.100775  PMID:23162300
  1,531 28 -
Lack of association between the G-660C polymorphism in the dopamine transporter gene (SLC6A3) and schizophrenia in the Iranian population
Ali M Foroughmand, Hamid Galehdari, Bentalhoda Tirband Dastgerdi, Saeed Reza Khatami, Maryam Haidari
May-August 2012, 18(2):222-225
DOI:10.4103/0971-6866.100773  PMID:23162299
  1,133 22 -
LETTERS TO THE EDITOR
Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals
Amit Kumar, Pradeep Kumar, Jitendra K Sahu
May-August 2012, 18(2):270-270
DOI:10.4103/0971-6866.100786  PMID:23162314
  1,029 53 -
Honey, chromosomal breakage and fanconi anemia
Somsri Wiwanitkit, Viroj Wiwanitkit
May-August 2012, 18(2):269-269
DOI:10.4103/0971-6866.100783  PMID:23162313
  875 25 -
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