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Lihadh Al-Gazali

Showing results (1-10 of 152) with videos related to

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Science (New York, N.Y.)|February 19, 2011
Genome-sequencing anniversary. Human genome sequencing: celebrating 10 yearsLihadh Al-Gazali
Saudi Medical Journal|July 9, 2003
BRCA1 and BRCA2 mutations in breast cancer patients from Saudi ArabiaSrdjan Denic, Lihadh Al-Gazali
Community Genetics|March 16, 2005
Genetics: global challenge, regional focus. Advances in community and preventive geneticsLihadh Al-Gazali, Valsa Eapen
International Journal of Molecular Medicine|November 14, 2002
Breast cancer, consanguinity, and lethal tumor genes: simulation of BRCA1/2 prevalence over 40 generationsSrdjan Denic, Lihadh Al-Gazali
Human Heredity|July 26, 2014
Consanguinity and dysmorphology in ArabsLihadh Al-Gazali, Hanan Hamamy
Human Mutation|May 4, 2010
Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE)Lihadh Al-Gazali, Bassam R Ali
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 23, 2013
A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2Nadia Akawi, Bassam Ali, Lihadh Al Gazali
BMJ (Clinical Research Ed.)|October 21, 2006
Genetic disorders in the Arab worldLihadh Al-Gazali, Hanan Hamamy, Shaikha Al-Arrayad
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 22, 2006
A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2Verena Matejas, Lihadh Al-Gazali, Iradj Amirlak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 9, 2012
A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataractNadia A Akawi, Bassam R Ali, Lihadh Al-Gazali
Pageof 16

Showing results (1-10 of 152) with videos related to

Sort By:
Pageof 16
Science (New York, N.Y.)|February 19, 2011
Genome-sequencing anniversary. Human genome sequencing: celebrating 10 yearsLihadh Al-Gazali
Saudi Medical Journal|July 9, 2003
BRCA1 and BRCA2 mutations in breast cancer patients from Saudi ArabiaSrdjan Denic, Lihadh Al-Gazali
Community Genetics|March 16, 2005
Genetics: global challenge, regional focus. Advances in community and preventive geneticsLihadh Al-Gazali, Valsa Eapen
International Journal of Molecular Medicine|November 14, 2002
Breast cancer, consanguinity, and lethal tumor genes: simulation of BRCA1/2 prevalence over 40 generationsSrdjan Denic, Lihadh Al-Gazali
Human Heredity|July 26, 2014
Consanguinity and dysmorphology in ArabsLihadh Al-Gazali, Hanan Hamamy
Human Mutation|May 4, 2010
Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE)Lihadh Al-Gazali, Bassam R Ali
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 23, 2013
A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2Nadia Akawi, Bassam Ali, Lihadh Al Gazali
BMJ (Clinical Research Ed.)|October 21, 2006
Genetic disorders in the Arab worldLihadh Al-Gazali, Hanan Hamamy, Shaikha Al-Arrayad
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 22, 2006
A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2Verena Matejas, Lihadh Al-Gazali, Iradj Amirlak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 9, 2012
A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataractNadia A Akawi, Bassam R Ali, Lihadh Al-Gazali
Pageof 16