Detalhe da pesquisa
1.
GALNS mutations in Indian patients with mucopolysaccharidosis IVA.
Am J Med Genet A
; 164A(11): 2793-801, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25252036
2.
Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South India.
Indian J Hum Genet
; 19(2): 165-70, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24019617
3.
Brahmarasayana protects against Ethyl methanesulfonate or Methyl methanesulfonate induced chromosomal aberrations in mouse bone marrow cells.
BMC Complement Altern Med
; 12: 113, 2012 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22853637
4.
Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type.
Indian J Hum Genet
; 18(3): 346-8, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23716945
5.
Recurrent and novel GLB1 mutations in India.
Gene
; 567(2): 173-81, 2015 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25936995
6.
Immunophenotyping of normal individuals classified on the basis of human dosha prakriti.
J Ayurveda Integr Med
; 5(1): 43-9, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24812475
7.
Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome.
J Hum Reprod Sci
; 6(2): 129-32, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24082654
8.
Single nucleotide polymorphisms of ADRB2 gene and their association with susceptibility for Plasmodium falciparum malaria and asthma in an Indian population.
Infect Genet Evol
; 20: 140-7, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24012958
9.
Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations.
Clin Dysmorphol
; 20(4): 205-209, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21716096