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Indian Journal of Human Genetics|September 11, 2013
Angiotensin II type 1 receptor A1166C gene polymorphism and essential hypertension in Calabar and Uyo cities, NigeriaMary Esien Kooffreh, Chiaka Ijeoma Anumudu, Roseline Duke, et al.Indian Journal of Human Genetics|September 11, 2013
The effect of FokI vitamin D receptor polymorphism on bone mineral density in Jordanian perimenopausal womenRaed M KananIndian Journal of Human Genetics|September 11, 2013
Genetic and environmental effects on age at menarche, and its relationship with reproductive health in twinsShayesteh Jahanfar, Munn-Sann Lye, Isthrinayagy S KrishnarajahIndian Journal of Human Genetics|September 11, 2013
Early diagnosis of co-existent ß-thalassemia and alkaptonuriaMoushumi Lodh, Joshi A KerkettaIndian Journal of Human Genetics|November 20, 2012
Chromosomal abnormalities and hormonal disorders of primary amenorrhea patients in EgyptFaeza El-DahtoryIndian Journal of Human Genetics|November 20, 2012
Molecular epidemiology of β-thalassemia in Pakistan: Far reaching implicationsSaqib H Ansari, Tahir S Shamsi, Mushtaq Ashraf, et al.Indian Journal of Human Genetics|November 20, 2012
Genetic counseling in carriers of reciprocal translocations involving two autosomesBahareh Pourjafari, Hamid Pour-Jafari, Marzieh Farimani, et al.Indian Journal of Human Genetics|November 20, 2012
Association of generalized aggressive periodontitis and ectrodactyly-ectodermal dysplasia-cleft syndromeRosamma Joseph, Sameera G NathIndian Journal of Human Genetics|August 1, 2013
Nucleotide sequence analysis of NIPBL gene in Indian Cornelia de Lange syndrome casesShailesh Bajaj, Suvidya Ranade, Prakash GambhirIndian Journal of Human Genetics|August 1, 2013
Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearingKarina Bezerra Salomão, Christiane Maria Ayo, Valter Augusto Della-RosaPageof 35