Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Roshan Colah

Showing results (31-40 of 57) with videos related to

Pageof 6
Sort By:
Prenatal Diagnosis|October 13, 2015
Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partnerManju Gorivale, Pratibha Sawant, Pallavi Mehta, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
A novel nine base deletion mutation in <i>NADH</i>-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-IIPrashant Warang, Prabhakar Kedar, S Sivanandam, et al.
Indian Journal of Human Genetics|September 15, 2010
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western IndiaNishi Madan, Satendra Sharma, S K Sood, et al.
International Journal of Laboratory Hematology|May 16, 2020
Prevalence of globin gene modifiers encountered in fetuses during antenatal diagnosis of hemoglobinopathiesPallavi Mehta, Pratibha Sawant, Manju Gorivale, et al.
Indian Journal of Pediatrics|April 8, 2016
Sickle Cell Disease in Central India: A Potentially Severe SyndromeDipty Jain, Vinit Warthe, Paridhi Dayama, et al.
Prenatal Diagnosis|May 21, 2005
Prenatal diagnosis of sickle syndromes in India: dilemmas in counsellingRoshan Colah, Reema Surve, Anita Nadkarni, et al.
European Journal of Haematology|June 14, 2012
Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian populationKhushnooma Italia, Pratibha Sawant, Reema Surve, et al.
Hematology (Amsterdam, Netherlands)|October 1, 2013
Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from IndiaPrashant Warang, Sona Nair, Anita Nadkarni, et al.
Molecular Biology Reports|September 8, 2017
Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotypePriya Hariharan, Madhavi Sawant, Manju Gorivale, et al.
Annals of Hematology|May 14, 2013
Molecular characterization of β-thalassemia in four communities in South Gujarat--codon 30 (G → A) a predominant mutation in the Kachhiya Patel communityDipal S Bhukhanvala, Khushnooma Italia, Pratibha Sawant, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|October 13, 2015
Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partnerManju Gorivale, Pratibha Sawant, Pallavi Mehta, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
A novel nine base deletion mutation in <i>NADH</i>-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-IIPrashant Warang, Prabhakar Kedar, S Sivanandam, et al.
Indian Journal of Human Genetics|September 15, 2010
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western IndiaNishi Madan, Satendra Sharma, S K Sood, et al.
International Journal of Laboratory Hematology|May 16, 2020
Prevalence of globin gene modifiers encountered in fetuses during antenatal diagnosis of hemoglobinopathiesPallavi Mehta, Pratibha Sawant, Manju Gorivale, et al.
Indian Journal of Pediatrics|April 8, 2016
Sickle Cell Disease in Central India: A Potentially Severe SyndromeDipty Jain, Vinit Warthe, Paridhi Dayama, et al.
Prenatal Diagnosis|May 21, 2005
Prenatal diagnosis of sickle syndromes in India: dilemmas in counsellingRoshan Colah, Reema Surve, Anita Nadkarni, et al.
European Journal of Haematology|June 14, 2012
Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian populationKhushnooma Italia, Pratibha Sawant, Reema Surve, et al.
Hematology (Amsterdam, Netherlands)|October 1, 2013
Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from IndiaPrashant Warang, Sona Nair, Anita Nadkarni, et al.
Molecular Biology Reports|September 8, 2017
Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotypePriya Hariharan, Madhavi Sawant, Manju Gorivale, et al.
Annals of Hematology|May 14, 2013
Molecular characterization of β-thalassemia in four communities in South Gujarat--codon 30 (G → A) a predominant mutation in the Kachhiya Patel communityDipal S Bhukhanvala, Khushnooma Italia, Pratibha Sawant, et al.
Pageof 6