Indian Journal of Human Genetics
Medknow Publications on behalf of Indian Society of Human Genetics
Explaining anthropometric variations in sickle cell disease requires a multidimensional approach
Mukherjee, Malay B.; Ghosh, Kanjaksha
An anthropometric and hematological comparison of sickle cell disease children from rural and urban areas
Nikhar, H S.; Meshram, S U.; Shinde, G B.
Prevalence of methylenetetrahydrofolate reductase C677T polymorphism in eastern Uttar Pradesh
Rai, Vandana; Yadav, Upendra; Kumar, Pradeep
Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population
Mittal, Rama D.; Mandal, Raju K.
Epistatic interactions in idiopathic pulmonary arterial hypertension
Vadapalli, Shivani; Satyanarayana, M L.; Chaitra, K L.; Rani, H Surekh.; Sastry, B.K.S.; Nallari, Pratibha
Molecular analysis of genetic variation in angiotensin I-converting enzyme identifies no association with sporting ability: First report from Indian population
Kothari, Sweta T.; Chheda, Pratiksha; Chatterjee, Leena; Das, Bibhu R.
Karyotypic findings in chronic myeloid leukemia cases undergoing treatment
Kaur, Anupam; Kaur, Simran Preet.; Singh, Amarjit; Singh, Jai Rup.
Inbreeding as a cause for deafness: Dadhkai study
Razdan, Sushil; Raina, Sunil Kumar.; Pandita, Kamal K.; Razdan, Shiveta; Nanda, Renu; Kaul, Rajni; Dogra, Sandeep
Prenatal sonographic evaluation and postnatal outcome of renal anomalies
Kumar, Manisha; Gupta, Usha; Thakur, Seema; Aggrawal, Shilpi; Meena, Jyoti; Sharma, Sumedha; Trivedi, Shubha S.
In silico prediction of exposure amino acid sequences of outer inflammatory protein A of
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Teymournejad, Omid; Mobarez, Ashraf M.; Hassan, Zuhair M.; Moazzeni, Seyed M.; Yakhchali, Bagher; Eskandari, Vajihe
SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India
D'Souza, Edna; Nair, Sona; Nadkarni, Anita; Ghosh, Kanjaksha; Colah, Roshan B.
Utility of MLPA in mutation analysis and carrier detection for Duchenne muscular dystrophy
Verma, Prashant K.; Dalal, Ashwin; Mittal, Balraj; Phadke, Shubha R.
The effect of aging on micronuclei frequency and proliferation in human peripheral blood lymphocytes
Orta, Tuncay; Günebakan, Süreyya
Genetic sensitivity to bitter taste of 6-n Propylthiouracil: A useful diagnostic aid to detect early childhood caries in pre-school children
Pidamale, Raghavendra; Sowmya, B; Thomas, Ann; Jose, Tony
A homozygous female hemophilia A
Nair, Preethi S.; Shetty, S; Ghosh, Kanjaksha
Effect of gene polymorphisms on periodontal diseases
Tarannum, Fouzia; Faizuddin, Mohamed
Genetic biomarkers of depression
Tamatam, Anand; Khanum, Farhath; Bawa, Amarinder Singh.
Science of breeding and heredity from ancient Persia to modern Iran
Kariminejad, Mohammad H.; Khorshidian, Ardeshir
Cytogenetic investigation of patients with primary amenorrhea
Laxmi, K Vijaya.; Babu, S J.; Dayakar, S; Mehrothra, R N.; Goud, Kalal I.
Wolf-Hirschhorn syndrome: A case demonstrated by a cytogenetic study
Pokale, Yamini S.; Jadhav, Ajinkya M.; Kate, Ushang
Familial germ cell tumor
Cyriac, Sanju; Rajendranath, Rejeev; Louis, A Robert.; Sagar, T G.
Methylenetetrahydrofolate reductase mutations, a genetic cause for familial recurrent neural tube defects
Yaliwal, Laxmi V.; Desai, Rathnamala M.
Cockayne syndrome-xeroderma pigmentosum complex with demyelination: A rare association
Singh, Usha Rani.; Asif, Shujaath; Kommu, Peter Prasanth Kumar.; D'Souza, Philomina
Dysmorphic features and congenital heart disease in chromosome 6q deletion: A short report
Nair, Sreelata; Varghese, Rini; Hashim, Sajeed; Scariah, Pappachan
A child with mosaicism for deletion (14)(q11.2q13)
Gamage, Thilini H.; Godapitiya, Imaya U.H..; Nanayakkara, Shakila; Jayasekara, Rohan W.; Dissanayake, Vajira H.W..
Trisomy 8 in leukemia: A GCRI experience
Bakshi, Sonal R.; Brahmbhatt, Manisha M.; Trivedi, Pina J.; Dalal, Esha N.; Patel, Dharmesh M.; Purani, Sejal S.; Shukla, Shilin N.; Shah, Pankaj M.; Patel, Prabhudas S.
Recombination in human leukocyte antigen region in two Asian Indian families
Mishra, Mahendra N.; Sharma, Ajay
Recollections of J.B.S. Haldane, with special reference to Human Genetics in India
Dronamraju, Krishna R.
A comparison of Fulani and Nadar HLA
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