Indian Journal of Human Genetics
Medknow Publications on behalf of Indian Society of Human Genetics
Is RBC discrimination index suitable for differentiating between α- and β- thalassemias?
Gorakshakar, Ajit C.; Colah, Roshan B.
Incidence of down syndrome: Hypotheses and reality
Vundinti, Babu Rao.; Ghosh, Kanjaksha
Evaluation of concentration and storage effects of mitomycin C in the diagnosis of Fanconi anemia among idiopatic aplastic anemia patients
Mozdarani, H; Ashtiani, K Abed.; Mohseni-Meybodi, A
A six-nucleotide deletion polymorphism in the casp8 promoter is associated with reduced risk of esophageal and gastric cancers in Kashmir valley
Malik, Manzoor Ahmad.; Zargar, Showkat Ali.; Mittal, Balraj
Cytogenetic and comorbidity profile of Down syndrome in Mansoura University Children's Hospital, Egypt
El-Gilany, Abdel-Hady; Yahia, Sohier; Shoker, Mohamed; El-Dahtory, Faeza
Genetic analysis of
gene polymorphisms in an Indian population
Umamaheswaran, Gurusamy; Praveen, Ramakrishnan G.; Arunkumar, Annan S.; Das, Ashok K.; Shewade, Deepak G.; Adithan, Chandrasekaran
Haptoglobin polymorphism among the tribal groups of southern Gujarat
Khurana, Priyanka; Aggarwal, Aastha; Huidrom, Suraj Singh.; Kshatriya, Gautam K.
Association of CYP3A5*3 polymorphism with development of acute leukemia
Rao, D Nageswara.; Manjula, G; Sailaja, K; Surekha, D; Raghunadharao, D; Rajappa, Senthil; Vishnupriya, S
Evaluation of DNA damage in agricultural workers exposed to pesticides using single cell gel electrophoresis (comet) assay
Kaur, Raminderjeet; Kaur, Satbir; Lata, Mukesh
Tracing disease gene(s) in non-syndromic clefts of orofacial region: HLA haplotypic linkage by analyzing the microsatellite markers: MIB, C1_2_5, C1_4_1, and C1_2_A
Rajendran, R; Shaikh, Saleem F.; Anil, Sukumaran
gene polymorphisms in the South Asian immigrant population in the United States
Henkhaus, Rebecca S.; Dodani, Sunita; Manzardo, Ann M.; Butler, Merlin G.
Risk conferred by FokI polymorphism of vitamin D receptor (VDR) gene for essential hypertension
Swapna, N; Vamsi, U Mohana.; Usha, G; Padma, T
A comparative study of hematological parameters of α and β thalassemias in a high prevalence zone: Saudi Arabia
Mehdi, Syed Riaz.; Al Dahmash, Badr Abdullah.
Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
Hamzi, Khalil; Tazzite, Amal; Nadifi, Sellama
Growth response of Egyptian children with idiopathic short stature during four years of growth hormone therapy
Ismail, Nagwa Abdallah.; Metwaly, Nermeen Salah Eldin.; El-Moguy, Fatma Ahmed.; Hafez, Mona Hassan.; Abd El Dayem, Soha M.; Farid, Tarek Mohamed.
Apoptosis and survival
Neural tube defects between folate metabolism and genetics
Alfarra, Helmi Y.; Alfarra, Sabreen R.; Sadiq, Mai F.
A comprehensive review on host genetic susceptibility to human papillomavirus infection and progression to cervical cancer
Refractory seizures with global developmental delay: A rare cause
Vinoth, P N.; Chacko, Betty; Xavier Scott, J Julius.; , Venkatasai
Ross operation in a neuro-cardio-facial-cutaneous syndrome patient
Zanjani, Keyhan S.; Zeinaloo, Ali Akbar.; Radmehr, Hassan
A novel mutation (4040-4045 nt. delA) in exon 14 of the factor VIII gene causing severe hemophilia A
Onsori, Habib; Feizi, Mohammad Ali Hosseinpour.; Feizi, Abbas Ali Hosseinpour.
Acute promyelocytic leukemia with unusual karyotype
Gowri, Mangala; Kousar Jahan, S K.; , Kavitha; , Prasannakumari; , Madhumathi; Appaji, L
Octaploidy in idiopathic thrombocytopenic purpura
Makroo, R N.; Chowdhry, Mohit; Mishra, Manoj; Srivastava, Priyanka; Fauzdar, Ashish
Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association
Kumar, Jeevan M.; Gowrishankar, Kalpana; Vasanthi, T; Kumar, R Ashok.; Jayasudha, T
Letter to the Editor
NQO1 C 609 T polymorphisms analyzed in a population from Kolkata, West Bengal
Mukherjee, Sanjit; Chaudhuri, Keya
Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder
Nagaveni, N B.; Umashankara, K V.
Goyal, Jagdish P.; Gupta, Anshul; Shah, Vijay B.
Null effect of p53 codon 72 polymorphism on recurrent pregnancy loss and recurrent implantation failure: A summative assessment
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