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Madiha Mohamed

Showing results (1-10 of 17) with videos related to

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Cureus|January 25, 2023
A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström SyndromeRania Snobar, Madiha Mohamed, Ahmed AlKamali, et al.
Cureus|September 20, 2024
A Rare Genetic Intersection: Down Syndrome With Coexisting Spinal Muscular AtrophyBhavna Gupta, Madiha Mohamed, Aman Sohal, et al.
European Journal of Medical Genetics|January 29, 2019
Expanded PCH1D phenotype linked to EXOSC9 mutationSami Bizzari, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
Cureus|October 16, 2023
Juvenile Ossifying Fibroma of the Nasal Bones: A Rare Cause of Chronic EpistaxisTaqwa Drdir, Theekshitha Kamalakannan, Madiha Mohamed, et al.
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|August 22, 2016
Marinesco-Sjögren Syndrome in an Emirati Child with a Novel Mutation in SIL1 Affecting the 5' Untranslated RegionPratibha Nair, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
Metabolic Brain Disease|May 26, 2016
Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosisPratibha Nair, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
European Journal of Medical Genetics|May 16, 2016
A novel nonsense GPSM2 mutation in a Yemeni family underlying Chudley-McCullough syndromeAbdul Rezzak Hamzeh, Pratibha Nair, Madiha Mohamed, et al.
Metabolic Brain Disease|February 13, 2018
Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2)Tasneem Obeid, Abdul Rezzak Hamzeh, Fatima Saif, et al.
BMC Medical Genetics|June 17, 2017
Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case reportFatma Bastaki, Pratibha Nair, Madiha Mohamed, et al.
BMC Pediatrics|January 21, 2017
A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAEAbdul Rezzak Hamzeh, Fatima Saif, Pratibha Nair, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Cureus|January 25, 2023
A Rare Cause of Infantile-Onset Cardiomyopathy With Ocular Manifestations: Alström SyndromeRania Snobar, Madiha Mohamed, Ahmed AlKamali, et al.
Cureus|September 20, 2024
A Rare Genetic Intersection: Down Syndrome With Coexisting Spinal Muscular AtrophyBhavna Gupta, Madiha Mohamed, Aman Sohal, et al.
European Journal of Medical Genetics|January 29, 2019
Expanded PCH1D phenotype linked to EXOSC9 mutationSami Bizzari, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
Cureus|October 16, 2023
Juvenile Ossifying Fibroma of the Nasal Bones: A Rare Cause of Chronic EpistaxisTaqwa Drdir, Theekshitha Kamalakannan, Madiha Mohamed, et al.
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|August 22, 2016
Marinesco-Sjögren Syndrome in an Emirati Child with a Novel Mutation in SIL1 Affecting the 5' Untranslated RegionPratibha Nair, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
Metabolic Brain Disease|May 26, 2016
Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosisPratibha Nair, Abdul Rezzak Hamzeh, Madiha Mohamed, et al.
European Journal of Medical Genetics|May 16, 2016
A novel nonsense GPSM2 mutation in a Yemeni family underlying Chudley-McCullough syndromeAbdul Rezzak Hamzeh, Pratibha Nair, Madiha Mohamed, et al.
Metabolic Brain Disease|February 13, 2018
Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2)Tasneem Obeid, Abdul Rezzak Hamzeh, Fatima Saif, et al.
BMC Medical Genetics|June 17, 2017
Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case reportFatma Bastaki, Pratibha Nair, Madiha Mohamed, et al.
BMC Pediatrics|January 21, 2017
A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAEAbdul Rezzak Hamzeh, Fatima Saif, Pratibha Nair, et al.
Pageof 2