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Indian Journal of Pediatrics
|
August 10, 2000
Biotinidase deficiency--a treatable entity
S Gulati, G R Passi, A Kumar, et al.
Indian Pediatrics
|
July 5, 2005
Cord blood analysis for prenatal diagnosis of thalassemia major and hemophilia A
I Panigrahi, R P H Ahmed, M Kannan, et al.
Indian Pediatrics
|
September 1, 1996
Clinical and enzyme studies in Gaucher disease
M Kaur, M Kabra, A Kher, et al.
Indian Journal of Pediatrics
|
May 24, 2001
Mitochondrial myopathy presenting as ataxia with dilated cardiomyopathy
S Gulati, A Das Gupta, M Kabra, et al.
Hematology (Amsterdam, Netherlands)
|
July 16, 2005
Do alpha deletions influence hydroxyurea response in thalassemia intermedia?
I Panigrahi, A Dixit, S Arora, et al.
The Indian Journal of Medical Research
|
November 1, 1996
Karyotyping of at risk fetuses by cordocentesis in advanced gestation
M Kabra, R Saxena, D Chinnappan, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 11, 2004
Novel missense mutation in the coagulation factor IX catalytic domain associated with severe haemophilia B--Factor IXDelhi
A Mahajan, A Sharma, S Chavali, et al.
Clinical Chemistry
|
July 1, 1978
Simultaneous determination of phosphatidylglycerol and the lecithin/sphingomyelin ratio in amniotic fluid
G R Gotelli, R E Stanfill, P M Kabra, et al.
Clinical Genetics
|
August 11, 2016
Nasopharyngeal teratoma, congenital diaphragmatic hernia and Dandy-Walker malformation - a yet uncharacterized syndrome
N Gupta, S Shastri, P K Singh, et al.
Clinical Chemistry
|
April 1, 1983
Liquid-chromatographic determination of tobramycin in serum with spectrophotometric detection
P M Kabra, P K Bhatnagar, M A Nelson, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 121) with videos related to
Sort By:
Page
of 13
Indian Journal of Pediatrics
|
August 10, 2000
Biotinidase deficiency--a treatable entity
S Gulati, G R Passi, A Kumar, et al.
Indian Pediatrics
|
July 5, 2005
Cord blood analysis for prenatal diagnosis of thalassemia major and hemophilia A
I Panigrahi, R P H Ahmed, M Kannan, et al.
Indian Pediatrics
|
September 1, 1996
Clinical and enzyme studies in Gaucher disease
M Kaur, M Kabra, A Kher, et al.
Indian Journal of Pediatrics
|
May 24, 2001
Mitochondrial myopathy presenting as ataxia with dilated cardiomyopathy
S Gulati, A Das Gupta, M Kabra, et al.
Hematology (Amsterdam, Netherlands)
|
July 16, 2005
Do alpha deletions influence hydroxyurea response in thalassemia intermedia?
I Panigrahi, A Dixit, S Arora, et al.
The Indian Journal of Medical Research
|
November 1, 1996
Karyotyping of at risk fetuses by cordocentesis in advanced gestation
M Kabra, R Saxena, D Chinnappan, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 11, 2004
Novel missense mutation in the coagulation factor IX catalytic domain associated with severe haemophilia B--Factor IXDelhi
A Mahajan, A Sharma, S Chavali, et al.
Clinical Chemistry
|
July 1, 1978
Simultaneous determination of phosphatidylglycerol and the lecithin/sphingomyelin ratio in amniotic fluid
G R Gotelli, R E Stanfill, P M Kabra, et al.
Clinical Genetics
|
August 11, 2016
Nasopharyngeal teratoma, congenital diaphragmatic hernia and Dandy-Walker malformation - a yet uncharacterized syndrome
N Gupta, S Shastri, P K Singh, et al.
Clinical Chemistry
|
April 1, 1983
Liquid-chromatographic determination of tobramycin in serum with spectrophotometric detection
P M Kabra, P K Bhatnagar, M A Nelson, et al.
Page
of 13