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Items: 5

1.

Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNA.

Bashyam MD, Chaudhary AK, Reddy EC, Devi AR, Savithri GR, Ratheesh R, Bashyam L, Mahesh E, Sen D, Puri R, Verma IC, Nampoothiri S, Vaidyanathan S, Chandrashekar MD, Kantheti P.

Mol Genet Metab. 2010 May;100(1):96-9. doi: 10.1016/j.ymgme.2010.01.016. Epub 2010 Feb 2. Erratum in: Mol Genet Metab. 2010 Aug;100(4):390. Verma, Inder C [corrected to Verma, Ishwar C].

PMID:
20188615
2.
3.

Molecular genetic analyses of beta-thalassemia in South India reveals rare mutations in the beta-globin gene.

Bashyam MD, Bashyam L, Savithri GR, Gopikrishna M, Sangal V, Devi AR.

J Hum Genet. 2004;49(8):408-13. Epub 2004 Jul 24.

PMID:
15278762
4.

Molecular genetics of familial hypertrophic cardiomyopathy (FHC).

Bashyam MD, Savithri GR, Kumar MS, Narasimhan C, Nallari P.

J Hum Genet. 2003;48(2):55-64. Review.

PMID:
12601548
5.

Molecular characterization of multidrug-resistant isolates of Mycobacterium tuberculosis from patients in North India.

Siddiqi N, Shamim M, Hussain S, Choudhary RK, Ahmed N, Prachee, Banerjee S, Savithri GR, Alam M, Pathak N, Amin A, Hanief M, Katoch VM, Sharma SK, Hasnain SE.

Antimicrob Agents Chemother. 2002 Feb;46(2):443-50.

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