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I C Verma

Showing results (91-100 of 280) with videos related to

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Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: Zmpste24. Disease: Restrictive dermopathyRenu Saxena, Sudha Kohli, I C Verma
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: PAX3. Disease: Waardenburg syndromeSudha Kohli, Renu Saxena, I C Verma
American Journal of Medical Genetics|July 1, 1994
Blepharophimosis, telecanthus, microstomia, and unusual ear anomaly (Simosa syndrome) in an infantM Suri, M Kabra, I C Verma
Birth Defects Original Article Series|January 1, 1975
An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomaliesI C Verma, S Bhargava, S Agarwal
The Indian Journal of Medical Research|February 1, 1986
Preliminary report on dermatoglyphic evidence for proto-australoid origin of muria gonds of Bastar (MP)I C Verma, R Elango, A Tomar
The Indian Journal of Medical Research|May 30, 1998
Utility of XY-amelogenin gene primers for detection of sex chromosomesM R Chowdhury, R Mathur, I C Verma
Pediatrics|February 1, 1981
Meconium passage in utero, fetal distress, and gestational ageI C Verma, S N Parida, S Thomas
Indian Journal of Pediatrics|September 1, 1982
Blood leucocyte changes for the early diagnosis of neonatal sepsisS N Parida, I C Verma, M Singh
Clinical Genetics|April 1, 1993
Phenotype of 49,XXYYYG P Das, A Shukla, I C Verma
Indian Journal of Pediatrics|July 1, 1993
Sphingomyelinase enzyme assay in Niemann-Pick diseaseM Kaur, G P Das, I C Verma
Pageof 28

Showing results (91-100 of 280) with videos related to

Sort By:
Pageof 28
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: Zmpste24. Disease: Restrictive dermopathyRenu Saxena, Sudha Kohli, I C Verma
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: PAX3. Disease: Waardenburg syndromeSudha Kohli, Renu Saxena, I C Verma
American Journal of Medical Genetics|July 1, 1994
Blepharophimosis, telecanthus, microstomia, and unusual ear anomaly (Simosa syndrome) in an infantM Suri, M Kabra, I C Verma
Birth Defects Original Article Series|January 1, 1975
An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomaliesI C Verma, S Bhargava, S Agarwal
The Indian Journal of Medical Research|February 1, 1986
Preliminary report on dermatoglyphic evidence for proto-australoid origin of muria gonds of Bastar (MP)I C Verma, R Elango, A Tomar
The Indian Journal of Medical Research|May 30, 1998
Utility of XY-amelogenin gene primers for detection of sex chromosomesM R Chowdhury, R Mathur, I C Verma
Pediatrics|February 1, 1981
Meconium passage in utero, fetal distress, and gestational ageI C Verma, S N Parida, S Thomas
Indian Journal of Pediatrics|September 1, 1982
Blood leucocyte changes for the early diagnosis of neonatal sepsisS N Parida, I C Verma, M Singh
Clinical Genetics|April 1, 1993
Phenotype of 49,XXYYYG P Das, A Shukla, I C Verma
Indian Journal of Pediatrics|July 1, 1993
Sphingomyelinase enzyme assay in Niemann-Pick diseaseM Kaur, G P Das, I C Verma
Pageof 28