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Anna Rajab

Showing results (1-10 of 49) with videos related to

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Journal of Community Genetics|July 4, 2013
Genetic services and testing in the Sultanate of Oman. Sultanate of Oman steps into modern geneticsAnna Rajab, I Al Rashdi, Q Al Salmi
Human Molecular Genetics|July 31, 2009
A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypesWibke Schwarzer, Florian Witte, Anna Rajab, et al.
American Journal of Medical Genetics|July 13, 2002
Heterogeneity for congenital generalized lipodystrophy in seventeen patients from OmanAnna Rajab, Kirsten Heathcote, Surendra Joshi, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Escobar variant with pursed mouth, creased tongue, ophthalmologic features, and scoliosis in 6 children from OmanAnna Rajab, K Hoffmann, A Ganesh, et al.
Reproductive Biomedicine Online|December 27, 2015
Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of OmanIntisar Al-Alawi, Tadakal Mallana Goud, Salma Al-Harasi, et al.
Thrombosis and Haemostasis|February 8, 2003
Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiencyMirko Pinotti, Rodney M Camire, Marcello Baroni, et al.
American Journal of Medical Genetics. Part A|November 3, 2007
A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasiaAnna Rajab, M Chiara Manzini, Ganeshwaran H Mochida, et al.
Journal of Medical Genetics|June 7, 2015
Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsyAnna Rajab, Markus Schuelke, Esther Gill, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from OmanAnna Rajab, U Kornak, B S Budde, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2Anna Rajab, Kimberly A Aldinger, Hisham Ali El-Shirbini, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Journal of Community Genetics|July 4, 2013
Genetic services and testing in the Sultanate of Oman. Sultanate of Oman steps into modern geneticsAnna Rajab, I Al Rashdi, Q Al Salmi
Human Molecular Genetics|July 31, 2009
A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypesWibke Schwarzer, Florian Witte, Anna Rajab, et al.
American Journal of Medical Genetics|July 13, 2002
Heterogeneity for congenital generalized lipodystrophy in seventeen patients from OmanAnna Rajab, Kirsten Heathcote, Surendra Joshi, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Escobar variant with pursed mouth, creased tongue, ophthalmologic features, and scoliosis in 6 children from OmanAnna Rajab, K Hoffmann, A Ganesh, et al.
Reproductive Biomedicine Online|December 27, 2015
Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of OmanIntisar Al-Alawi, Tadakal Mallana Goud, Salma Al-Harasi, et al.
Thrombosis and Haemostasis|February 8, 2003
Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiencyMirko Pinotti, Rodney M Camire, Marcello Baroni, et al.
American Journal of Medical Genetics. Part A|November 3, 2007
A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasiaAnna Rajab, M Chiara Manzini, Ganeshwaran H Mochida, et al.
Journal of Medical Genetics|June 7, 2015
Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsyAnna Rajab, Markus Schuelke, Esther Gill, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from OmanAnna Rajab, U Kornak, B S Budde, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2Anna Rajab, Kimberly A Aldinger, Hisham Ali El-Shirbini, et al.
Pageof 5