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Results of search for 'au:"Arunkumar, Jambulingam"'
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Authors
Arunkumar, Jambulingam
Aung, Tin
Hemadevi, Boomiraj
Lesaffre, Corinne
Mehta, Jodhbir Singh
Prajna, Namperumalsamy V
Prajna, Namperumalsamy Venkatesh
Prajna, Venkatesh
Srinivasan, Muthaiah
Srinivasan, Muthiah
Sundaresan, Periasamy
Tan, Donald T
Veitia, Reiner A
Vithana, Eranga N
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Topics
Adolescent
Adult
Amino Acid Sequence
Anion Transport Proteins
Antiporters
Audiometry
Base Sequence
Child
Child, Preschool
Corneal Dystrophies, Hereditary
Endothelium, Corneal
Female
Genotype
Humans
India
Male
Molecular Sequence Data
Mutation
Pedigree
genetics
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1.
Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India.
[electronic resource]
by
Hemadevi, Boomiraj
Srinivasan, Muthiah
Arunkumar, Jambulingam
Prajna, Namperumalsamy V
Sundaresan, Periasamy
Producer:
20100603
In:
BMC ophthalmology
vol. 10
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2.
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy.
[electronic resource]
by
Hemadevi, Boomiraj
Veitia, Reiner A
Srinivasan, Muthiah
Arunkumar, Jambulingam
Prajna, Namperumalsamy Venkatesh
Lesaffre, Corinne
Sundaresan, Periasamy
Producer:
20080522
In:
Archives of ophthalmology (Chicago, Ill. : 1960)
vol. 126
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3.
Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene.
[electronic resource]
by
Mehta, Jodhbir Singh
Hemadevi, Boomiraj
Vithana, Eranga N
Arunkumar, Jambulingam
Srinivasan, Muthaiah
Prajna, Venkatesh
Tan, Donald T
Aung, Tin
Sundaresan, Periasamy
Producer:
20100507
In:
Cornea
vol. 29
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