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Anna Rajab

Showing results (11-20 of 49) with videos related to

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Cytogenetic and Genome Research|March 5, 2026
Familial Robertsonian Translocation, rob(14;21), with high risk for Down syndromeAnna Rajab, Heidemarie Neitzel, Jenny Jalali, et al.
Reproductive Biomedicine Online|March 21, 2009
Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of OmanTadakal Mallana Goud, Salma Mohammed Al Harassi, Kamla Khalfan Al Salmani, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|October 31, 2015
Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/ Adult Acute Lymphoblastic Leukemia in Omani PatientsTadakal Mallana Goud, Kamla Khalfan Al Salmani, Salma Mohammed Al Harasi, et al.
Hemoglobin|April 1, 2010
Extended molecular spectrum of beta- and alpha-thalassemia in OmanSuha M Hassan, Nishat Hamza, Fatma Jaffer Al-Lawatiya, et al.
Diabetes|March 28, 2002
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple lociKirsten Heathcote, Anna Rajab, Jocelyne Magré, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2004
Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvementHolger Thiele, Masahiro Sakano, Hiroshi Kitagawa, et al.
American Journal of Human Genetics|August 27, 2013
Mutations in DDX59 implicate RNA helicase in the pathogenesis of orofaciodigital syndromeHanan E Shamseldin, Anna Rajab, Amal Alhashem, et al.
Saudi Medical Journal|December 29, 2005
Incidence of chromosome abnormalities in the Sultanate of OmanMallana T Goud, Salma M Al-Harassi, Shafiya A Al-Khalili, et al.
American Journal of Medical Genetics. Part A|June 9, 2006
An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardationAnna Rajab, Seung-Yun Yoo, Aiman Abdulgalil, et al.
Bone|May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Cytogenetic and Genome Research|March 5, 2026
Familial Robertsonian Translocation, rob(14;21), with high risk for Down syndromeAnna Rajab, Heidemarie Neitzel, Jenny Jalali, et al.
Reproductive Biomedicine Online|March 21, 2009
Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of OmanTadakal Mallana Goud, Salma Mohammed Al Harassi, Kamla Khalfan Al Salmani, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|October 31, 2015
Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/ Adult Acute Lymphoblastic Leukemia in Omani PatientsTadakal Mallana Goud, Kamla Khalfan Al Salmani, Salma Mohammed Al Harasi, et al.
Hemoglobin|April 1, 2010
Extended molecular spectrum of beta- and alpha-thalassemia in OmanSuha M Hassan, Nishat Hamza, Fatma Jaffer Al-Lawatiya, et al.
Diabetes|March 28, 2002
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple lociKirsten Heathcote, Anna Rajab, Jocelyne Magré, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2004
Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvementHolger Thiele, Masahiro Sakano, Hiroshi Kitagawa, et al.
American Journal of Human Genetics|August 27, 2013
Mutations in DDX59 implicate RNA helicase in the pathogenesis of orofaciodigital syndromeHanan E Shamseldin, Anna Rajab, Amal Alhashem, et al.
Saudi Medical Journal|December 29, 2005
Incidence of chromosome abnormalities in the Sultanate of OmanMallana T Goud, Salma M Al-Harassi, Shafiya A Al-Khalili, et al.
American Journal of Medical Genetics. Part A|June 9, 2006
An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardationAnna Rajab, Seung-Yun Yoo, Aiman Abdulgalil, et al.
Bone|May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.
Pageof 5