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I C Verma

Showing results (191-200 of 280) with videos related to

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Indian Journal of Pediatrics|June 1, 2000
Cytogenetics investigation in childhood chronic myeloid leukemiaD Chinnappan, I C Verma, V P Choudhry, et al.
The Indian Journal of Medical Research|November 1, 1983
HLA linkage to 21-hydroxylase congenital adrenal hyperplasiaA R Mathews, I C Verma, P S Menon, et al.
Indian Pediatrics|September 1, 1994
Jarcho-Levin syndromeM Suri, Madhulika, H Pemde, et al.
Indian Journal of Pediatrics|May 1, 1981
Perinatal mortality-incidence and effect of various maternal factors, Part IR K Puri, I C Verma, P Choudhury, et al.
The Indian Journal of Medical Research|October 1, 1984
Cord blood prolactin in normal & abnormal deliveriesS Thomas, P S Menon, O Singh, et al.
The Indian Journal of Medical Research|December 1, 1996
Delta F 508 molecular mutation in Indian children with cystic fibrosisM Kabra, M Ghosh, S K Kabra, et al.
Indian Pediatrics|June 1, 1975
Clinical profile in three patients with Beckwith-Wiedemann syndromeI C Verma, H L Goswami, M Rohtagi, et al.
The Indian Journal of Medical Research|March 1, 1981
Developmental milestones of Down's syndrome patients in north IndiaP S Menon, H P Sachdev, I C Verma, et al.
Indian Pediatrics|May 1, 1975
Prenatal diagnosis of genetic disordersI C Verma, R Joseph, K Verma, et al.
Human Mutation|January 1, 1994
A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian probandP K Jain, A M Dozy, I C Verma, et al.
Pageof 28

Showing results (191-200 of 280) with videos related to

Sort By:
Pageof 28
Indian Journal of Pediatrics|June 1, 2000
Cytogenetics investigation in childhood chronic myeloid leukemiaD Chinnappan, I C Verma, V P Choudhry, et al.
The Indian Journal of Medical Research|November 1, 1983
HLA linkage to 21-hydroxylase congenital adrenal hyperplasiaA R Mathews, I C Verma, P S Menon, et al.
Indian Pediatrics|September 1, 1994
Jarcho-Levin syndromeM Suri, Madhulika, H Pemde, et al.
Indian Journal of Pediatrics|May 1, 1981
Perinatal mortality-incidence and effect of various maternal factors, Part IR K Puri, I C Verma, P Choudhury, et al.
The Indian Journal of Medical Research|October 1, 1984
Cord blood prolactin in normal & abnormal deliveriesS Thomas, P S Menon, O Singh, et al.
The Indian Journal of Medical Research|December 1, 1996
Delta F 508 molecular mutation in Indian children with cystic fibrosisM Kabra, M Ghosh, S K Kabra, et al.
Indian Pediatrics|June 1, 1975
Clinical profile in three patients with Beckwith-Wiedemann syndromeI C Verma, H L Goswami, M Rohtagi, et al.
The Indian Journal of Medical Research|March 1, 1981
Developmental milestones of Down's syndrome patients in north IndiaP S Menon, H P Sachdev, I C Verma, et al.
Indian Pediatrics|May 1, 1975
Prenatal diagnosis of genetic disordersI C Verma, R Joseph, K Verma, et al.
Human Mutation|January 1, 1994
A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian probandP K Jain, A M Dozy, I C Verma, et al.
Pageof 28