On the Variability of Middle Phalangeal Hair Among Indian Populations

1965 ◽  
Vol 95 (1) ◽  
pp. 115 ◽  
Author(s):  
Pratap Chandra Dutta
Keyword(s):  
Indian Populations

Serum Albumin Variation in Indian Populations

Vox Sanguinis ◽  
1971 ◽  
Vol 21 (5) ◽  
pp. 462-464
Author(s):  
E.M. McDermid
Keyword(s):  
Serum Albumin ◽  
Indian Populations

Suggestive evidence of association of C-159T functional polymorphism of the CD14 gene with atopic asthma in northern and northwestern Indian populations

2004 ◽  
Vol 56 (7) ◽  
pp. 544-547 ◽  
Author(s):  
Mamta Sharma ◽  
Jyotsna Batra ◽  
U. Mabalirajan ◽  
Sangeeta Goswami ◽  
Dipyaman Ganguly ◽  
...  
Keyword(s):  
Atopic Asthma ◽  
Functional Polymorphism ◽  
Indian Populations ◽  
Suggestive Evidence ◽  
Cd14 Gene

Complex genetic origin of Indian populations and its implications

2012 ◽  
Vol 37 (5) ◽  
pp. 911-919 ◽  
Author(s):  
Rakesh Tamang ◽  
Lalji Singh ◽  
Kumarasamy Thangaraj
Keyword(s):  
Genetic Origin ◽  
Indian Populations

Dopamine transporter (DAT1) VNTR polymorphism in 12 Indian populations

2009 ◽  
Vol 30 (6) ◽  
pp. 487-493 ◽  
Author(s):  
L. V. K. S. Bhaskar ◽  
Kumarasamy Thangaraj ◽  
Connie J. Mulligan ◽  
Samiksha Wasnik ◽  
Amrita Nandan ◽  
...  
Keyword(s):  
Dopamine Transporter ◽  
Indian Populations ◽  
Vntr Polymorphism

Genetics Landscape of Nonsyndromic Hearing Loss in Indian Populations

2021 ◽  
Author(s):  
Manisha Ray ◽  
Saurav Sarkar ◽  
Mukund Namdev Sable
Keyword(s):  
Hearing Loss ◽  
Gap Junction ◽  
Genetic Heterogeneity ◽  
Target Gene ◽  
Indian Population ◽  
Nonsyndromic Hearing Loss ◽  
Indian Populations ◽  
Chronic Disorder

AbstractCongenital nonsyndromic hearing loss (NSHL) has been considered as one of the most prevalent chronic disorder in children. It affects the physical and mental conditions of a large children population worldwide. Because of the genetic heterogeneity, the identification of target gene is very challenging. However, gap junction β-2 (GJB2) is taken as the key gene for hearing loss, as its involvement has been reported frequently in NSHL cases. This study aimed to identify the association of GJB2 mutants in different Indian populations based on published studies in Indian population. This will provide clear genetic fundamental of NSHL in Indian biogeography, which would be helpful in the diagnosis process.

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