Indian Journal of Human Genetics - oalib

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Indian Journal of Human Genetics

ISSN Print: 0971-6866

ISSN Online:

主页: http://www.ijhg.com/

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Phenotypic correlations in a patient with ring chromosome 22

Demirhan Osman,Tun？ Erdal

Genetics in public health: Rarely explored

Aswini Y,Varun S

Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India

Madan Nishi,Sharma Satendra,Sood S,Colah Roshan

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

Screening for beta thalassaemia

Petrou Mary

The NQO1 allelic frequency in hindu population of central India varies from that of other Asian populations

Parihar Sher,Chauhan U

Integration of modern genetic knowledge and technology into public health in India

Ghosh Kanjaksha,Gorakshakar Ajit

Significance of t (8: 14) in CLL?

Lakshmaiah K,Tejinder S,Kumari Prasanna,Gowri Mangala

Bone age is the best predictor of growth response to recombinant human growth hormone in Turner′s syndrome

Ismail Nagwa,Metwaly Nermeen,El-Moguy Fatma,Hafez Mona

Defining genetic architecture of the populations in the Indian subcontinent: Impact of human leukocyte antigen diversity studies

Mehra N

Caspase 8 gene variants in healthy North Indian population and comparison with worldwide ethnic group variations

George Ginu,Mittal Rama

Oculo-facio-cardio-dental syndrome in a girl and her mother

Rudrappa Sudha,Kumar Rajendra,Kumar G

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

Mukherjee Malay,Nadkarni Anita,Gorakshakar Ajit,Ghosh Kanjaksha

Indian Journal of Human Genetics in PubMed: Cautious but confident steps

Ghosh Kanjaksha

Opportunity for natural selection among some selected population groups of Northeast India

Das Farida,Sikdar Mithun

Heritability estimation of conventional cardiovascular disease risk factors in Asian Indian families: The Calcutta family study

Ghosh Arnab,Dutta Rupak,Sarkar Angshuman

Association of polymorphisms in leptin receptor gene with obesity and type 2 diabetes in the local population of Coimbatore

Murugesan Devi,Arunachalam Thirunavukkarasu,Ramamurthy Viraragavan,Subramanian Selvi

Pharmacogenomics of pediatric asthma

Gupta Sarika,Awasthi Shally

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

Investigation of chromosomal aberrations in Egyptian hepatocellular carcinoma patients by fluorescence in situ hybridization

Aly Magdy,Bahnassy Abeer,Abdel-Rahman Zekri

Glanzmann′s thrombasthenia and molecular mimicry

Wiwanitkit Viroj

A rare case of congenital heart disease with ambiguous genitalia

Lingaiah Kusuma,Parshwanath Bharath,Mysore Savitha,Krishnamurthy Balasundaram

Gly460Trp polymorphism of the ADD1 gene and essential hypertension in an Indian population: A meta-analysis on hypertension risk

Ramu P,Umamaheswaran G,Shewade D,Swaminathan R

Sickle cell hemoglobinopathies in district Bhopal

Dangi C. B. S.,Sajid M,Sawke G,Ambhore J

Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy

Tanjore Reena,RangaRaju Advithi,Vadapalli Shivani,Remersu Sushant

Ataxia telangiectasia: Family management

Seshachalam Arun,Cyriac Sanju,Reddy Neelesh,Gnana Sagar

Dandy-Walker malformation: An incidental finding

Tadakamadla Jyothi,Kumar Santhosh,Mamatha G

Genetic assessment of serological and biochemical markers in Bharia tribe of Chhindwara district of Madhya Pradesh

Chaudhary Ruchira,Sharma Gunjan

Triploidy in a fetus following amniocentesis referred for maternal serum screening test at second trimester

Bagherizadeh E,Oveisi M,Hadipour Z,Saremi A

Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?

Hamzi Khalil,Itto Afaf,Nassereddine Sanaa,Nadifi Sellama

Autism and X-linked hypophosphatemia: A possible association?

Joel Vermeersch,Hans Hellemans,Dirk Deboutte

Dominant inheritance and intra-familial variations in the association of Sturge-Weber and Klippel-Trenaunay-Weber syndromes

Pereira de Godoy Jose,Fett-Conte Agnes

Complexities and similarities of HLA antigen distribution in Asian subcontinent

Shankarkumar U

A Sri Lankan child with 49,XXXXY syndrome

Dissanayake Vajira,Bandarage Palinda,Pedurupillay Christeen,Jayasekara Rohan

Haplotype diversity and linkage disequilibrium at the DRD2 locus among the tribes of western and southern regions of India

Aggarwal Aastha,Gauniyal Mansi,Pattanayak Ipsa,Kshatriya Gautam

Null association between ACE gene I/D polymorphism and diabetic nephropathy among multiethnic Malaysian subjects

Jayapalan Jaime,Muniandy Sekaran,Chan Siew

Congenital malformations at birth in Central India: A rural medical college hospital based data

Taksande Amar,Vilhekar Krishna,Chaturvedi Pushpa,Jain Manish

Antiplatelet antibodies in cases of Glanzmann′s thrombasthenia with and without a history of multiple platelet transfusion

Ghosh Kanjaksha,Kulkarni B,Shetty S,Nair S

Genetic studies in children with intellectual disability and autistic spectrum of disorders

Balasubramanian Bhanumathi,Bhatt Chetna,Goyel Neelam

Frequency of fokI and taqI polymorphism of vitamin D receptor gene in Indian population and its association with 25-hydroxyvitamin D levels

Bhanushali Aparna,Lajpal Namrata,Kulkarni Smita,Chavan Sandeep

A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experience

Trivedi P,Patel P,Brahmbhatt M,Patel B

Microsatellite diversity among the primitive tribes of India

Mukherjee Malay,Tripathy V,Colah R,Solanki P

APO-1/Fas gene: Structural and functional characteristics in systemic lupus erythematosus and other autoimmune diseases

Singh Richa,Pradhan Vandana,Patwardhan Manisha,Ghosh K

G691S/S904S polymorphism in the RET protooncogene of a 25-year-old medical student with bilateral pheochromocytoma

Arneth Borros

Linkage analysis of three families with arrythmogenic right ventricular cardiomyopathy in India

Dokuparthi Maithili,Pamuru Pranathi,Oruganti Sai,Calambur Narsimhan

Iranian human genome project: Overview of a research process among Iranian ethnicities

Banihashemi Kambiz

Chromosomal abnormalities associated with mental retardation in female subjects

Dutta Samikshan,Shaw Jyoti,Sinha Swagata,Mukhopadhyay Kanchan

In vitro up-regulation of expression of GITR on human CD8 + cells

Thanavala Yasmin

Weaver syndrome: A report of a rare genetic syndrome

Bansal Nitin,Bansal Amit

MTHFR Gene variants C677T, A1298C and association with Down syndrome: A case-control study from South India

Cyril Cyrus,Rai Padmalatha,Chandra N,Gopinath P

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