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Shazia Subhani

Showing results (1-10 of 15) with videos related to

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Journal of Diabetes Science and Technology|December 7, 2010
Design and development of a web-based Saudi National Diabetes RegistryShazia Subhani, Khalid Al-Rubeaan
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|October 30, 2008
Pattern of cleft lip and palate in hospital-based population in Saudi Arabia: retrospective studyAziza Aljohar, Kandasamy Ravichandran, Shazia Subhani
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|May 9, 2002
A web-based cleft lip and palate registryJ Burton Douglass, Susan Becker, Shazia Subhani, et al.
Teratology|February 22, 2002
Design and development of an Internet registry for congenital heart defectsWajeeh Mitri, Amy L Sandridge, Shazia Subhani, et al.
The International Journal of Biostatistics|October 5, 2011
Estimation of modified concordance ratio in sib-pairs: effect of consanguinity on the risk of congenital heart diseasesMohamed M Shoukri, Allan Donner, Nadia Abdalla Dessouky, et al.
Genome Medicine|June 21, 2023
The clinical utility of rapid exome sequencing in a consanguineous populationDorota Monies, Ewa Goljan, , et al.
Frontiers in Medicine|August 16, 2021
Whole-Genome Sequencing Reveals Exonic Variation of <i>ASIC5</i> Gene Results in Recurrent Pregnancy LossNourah H Al Qahtani, Sayed AbdulAzeez, Noor B Almandil, et al.
Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.
Scientific Reports|March 6, 2019
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's DiseaseEman Al Yemni, Dorota Monies, Thamer Alkhairallah, et al.
Scientific Reports|July 20, 2017
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi familiesBashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Diabetes Science and Technology|December 7, 2010
Design and development of a web-based Saudi National Diabetes RegistryShazia Subhani, Khalid Al-Rubeaan
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|October 30, 2008
Pattern of cleft lip and palate in hospital-based population in Saudi Arabia: retrospective studyAziza Aljohar, Kandasamy Ravichandran, Shazia Subhani
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|May 9, 2002
A web-based cleft lip and palate registryJ Burton Douglass, Susan Becker, Shazia Subhani, et al.
Teratology|February 22, 2002
Design and development of an Internet registry for congenital heart defectsWajeeh Mitri, Amy L Sandridge, Shazia Subhani, et al.
The International Journal of Biostatistics|October 5, 2011
Estimation of modified concordance ratio in sib-pairs: effect of consanguinity on the risk of congenital heart diseasesMohamed M Shoukri, Allan Donner, Nadia Abdalla Dessouky, et al.
Genome Medicine|June 21, 2023
The clinical utility of rapid exome sequencing in a consanguineous populationDorota Monies, Ewa Goljan, , et al.
Frontiers in Medicine|August 16, 2021
Whole-Genome Sequencing Reveals Exonic Variation of <i>ASIC5</i> Gene Results in Recurrent Pregnancy LossNourah H Al Qahtani, Sayed AbdulAzeez, Noor B Almandil, et al.
Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.
Scientific Reports|March 6, 2019
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's DiseaseEman Al Yemni, Dorota Monies, Thamer Alkhairallah, et al.
Scientific Reports|July 20, 2017
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi familiesBashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, et al.
Pageof 2