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Indian Journal of Human Genetics
Medknow Publications on behalf of Indian Society of Human Genetics
ISSN:
0971-6866
EISSN:
0971-6866
this issue
year
vol
number
2010
16
03
Available Articles
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Page No.
Author
Type
Editorial
Defining genetic architecture of the populations in the Indian subcontinent: Impact of human leukocyte antigen diversity studies
Mehra, N. K.
Research Article
Bone age is the best predictor of growth response to recombinant human growth hormone in
Turner's syndrome
Ismail, Nagwa Abdallah; Metwaly, Nermeen Salah Eldin; El-Moguy, Fatma Ahmed; Hafez, Mona Hassan; Abd El Dayem, Soha M.; Farid, Tarek Mohamed
Genetic assessment of serological and biochemical markers in Bharia tribe of Chhindwara district of Madhya Pradesh
Chaudhary, Ruchira; Sharma, Gunjan
The
NQO1
allelic frequency in hindu population of central India varies from that of other Asian populations
Parihar, Sher S.; Chauhan, U. K.
Methionine synthase polymorphisms (
MTR 2756
A>G and
MTR 2758 C>G
) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan
Al Farra, Helmi Yousif.
Caspase 8 gene variants in healthy North Indian population and comparison with worldwide ethnic group variations
George, Ginu P.; Mittal, Rama D.
Molecular analysis of human leukocyte antigen class I and class II allele frequencies and haplotype distribution in Pakistani population
Moatter, T.; Aban, M.; Tabassum, S.; Shaikh, U.; Pervez, S.
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India
Mukherjee, Malay B.; Nadkarni, Anita H.; Gorakshakar, Ajit C.; Ghosh, Kanjaksha; Mohanty, Dipika; Colah, Roshan B.
Special Article
Complexities and similarities of HLA antigen distribution in Asian subcontinent
Shankarkumar, U.
Review Article
Pharmacogenomics of pediatric asthma
Gupta, Sarika; Awasthi, Shally
Case Report
A Sri Lankan child with 49,XXXXY syndrome
Dissanayake, Vajira H.W.; Bandarage, Palinda; Pedurupillay, Christeen R.J.; Jayasekara, Rohan W.
A rare case of congenital heart disease with ambiguous genitalia
Lingaiah, Kusuma; Parshwanath, Bharath A.; Mysore, Savitha R.; Krishnamurthy, Balasundaram; Ramachandra, Nallur B.
Oculo-facio-cardio-dental syndrome in a girl and her mother
Rudrappa, Sudha; Kumar, Rajendra; Kumar, G. S.
Prader-Willi syndrome: Methylation study or fluorescence
in situ
hybridization first?
Hamzi, Khalil; Itto, Afaf Ben.; Nassereddine, Sanaa; Nadifi, Sellama
Report
Congenital malformations at birth in Central India: A rural medical college hospital based data
Taksande, Amar; Vilhekar, Krishna; Chaturvedi, Pushpa; Jain, Manish
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