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A Radha

Showing results (31-40 of 40) with videos related to

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Prenatal Diagnosis|April 29, 2008
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversionK Prabhakara, Damien L Bruno, Priya Padman, et al.
Biological Psychiatry|May 2, 2002
Diminished chaos of heart rate time series in patients with major depressionVikram Kumar Yeragani, K A Radha Krishna Rao, M Ramesh Smitha, et al.
International Journal of Medicinal Mushrooms|November 14, 2022
Hepatoprotective Constituents of Macrocybe gigantea (Agaricomycetes) from IndiaS Nagul Kumar, K Buvanesvaragurunathan, R Govindaraj, et al.
Journal of Cellular Biochemistry|May 18, 2012
Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1βMurali D Bashyam, Ajay K Chaudhary, Manjari Sinha, et al.
Molecular Genetics and Metabolism|March 2, 2010
Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNAMurali D Bashyam, Ajay K Chaudhary, E Chandrakanth Reddy, et al.
American Journal of Medical Genetics. Part A|May 20, 2015
Novel and recurrent mutations in WISP3 and an atypical phenotypeGandham SriLakshmi Bhavani, Hitesh Shah, Ashwin B Dalal, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosisSonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
Journal of Neurology|May 10, 2019
Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patientsAparna Ganapathy, Avshesh Mishra, Megha Rani Soni, et al.
American Journal of Medical Genetics. Part A|October 2, 2012
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorderSonja A de Munnik, Barto J Otten, Jeroen Schoots, et al.
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Showing results (31-40 of 40) with videos related to

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You have reached the last page of results.This site can display upto 40 results.
Prenatal Diagnosis|April 29, 2008
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversionK Prabhakara, Damien L Bruno, Priya Padman, et al.
Biological Psychiatry|May 2, 2002
Diminished chaos of heart rate time series in patients with major depressionVikram Kumar Yeragani, K A Radha Krishna Rao, M Ramesh Smitha, et al.
International Journal of Medicinal Mushrooms|November 14, 2022
Hepatoprotective Constituents of Macrocybe gigantea (Agaricomycetes) from IndiaS Nagul Kumar, K Buvanesvaragurunathan, R Govindaraj, et al.
Journal of Cellular Biochemistry|May 18, 2012
Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1βMurali D Bashyam, Ajay K Chaudhary, Manjari Sinha, et al.
Molecular Genetics and Metabolism|March 2, 2010
Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNAMurali D Bashyam, Ajay K Chaudhary, E Chandrakanth Reddy, et al.
American Journal of Medical Genetics. Part A|May 20, 2015
Novel and recurrent mutations in WISP3 and an atypical phenotypeGandham SriLakshmi Bhavani, Hitesh Shah, Ashwin B Dalal, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosisSonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
Journal of Neurology|May 10, 2019
Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patientsAparna Ganapathy, Avshesh Mishra, Megha Rani Soni, et al.
American Journal of Medical Genetics. Part A|October 2, 2012
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorderSonja A de Munnik, Barto J Otten, Jeroen Schoots, et al.
Pageof 4