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Journal of Pediatric Genetics
|
August 12, 2017
Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia
Nagwa E A Gaboon, Khadijah H Bakur, Alaa Y Edrees, et al.
Journal of Pediatric Genetics
|
February 26, 2019
Erratum: Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia
Nagwa E A Gaboon, Khadijah H Bakur, Alaa Y Edrees, et al.
Turkish Journal of Medical Sciences
|
March 7, 2017
A novel mutation in exon 1 of GATA4 in Egyptian patients with congenital heart disease
Olfat Shaker, Salwa Omran, Eman Sharaf, et al.
Turkish Journal of Medical Sciences
|
March 21, 2015
Structural chromosomal abnormalities in couples with recurrent abortion in Egypt
Nagwa E A Gaboon, Ahmed Ramy Mohamed, Solaf M Elsayed, et al.
Frontiers in Pediatrics
|
July 12, 2019
A Novel Homozygous Frameshift Mutation in <i>CCN6</i> Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family
Nagwa E A Gaboon, Asia Parveen, Ahmed El Beheiry, et al.
The Journal of Dermatology
|
April 10, 2015
Case of Sjögren-Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis
Nagwa E A Gaboon, Musharraf Jelani, Mona M Almramhi, et al.
Frontiers in Pediatrics
|
August 9, 2020
A Novel Homozygous Frameshift Variant in <i>DYM</i> Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients
Nagwa E A Gaboon, Asia Parveen, Khaled A Ahmad, et al.
Journal of Molecular Neuroscience : MN
|
October 4, 2024
Clinical and Molecular Profiles of a Cohort of Egyptian Patients with Collagen VI-Related Dystrophy
Wessam E Sharaf-Eldin, Karima Rafat, Mahmoud Y Issa, et al.
Saudi Journal of Biological Sciences
|
January 1, 2020
Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects
Nagwa E A Gaboon, Babajan Banaganapalli, Khalidah Nasser, et al.
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of 1
Search research articles
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Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Journal of Pediatric Genetics
|
August 12, 2017
Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia
Nagwa E A Gaboon, Khadijah H Bakur, Alaa Y Edrees, et al.
Journal of Pediatric Genetics
|
February 26, 2019
Erratum: Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia
Nagwa E A Gaboon, Khadijah H Bakur, Alaa Y Edrees, et al.
Turkish Journal of Medical Sciences
|
March 7, 2017
A novel mutation in exon 1 of GATA4 in Egyptian patients with congenital heart disease
Olfat Shaker, Salwa Omran, Eman Sharaf, et al.
Turkish Journal of Medical Sciences
|
March 21, 2015
Structural chromosomal abnormalities in couples with recurrent abortion in Egypt
Nagwa E A Gaboon, Ahmed Ramy Mohamed, Solaf M Elsayed, et al.
Frontiers in Pediatrics
|
July 12, 2019
A Novel Homozygous Frameshift Mutation in <i>CCN6</i> Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family
Nagwa E A Gaboon, Asia Parveen, Ahmed El Beheiry, et al.
The Journal of Dermatology
|
April 10, 2015
Case of Sjögren-Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis
Nagwa E A Gaboon, Musharraf Jelani, Mona M Almramhi, et al.
Frontiers in Pediatrics
|
August 9, 2020
A Novel Homozygous Frameshift Variant in <i>DYM</i> Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients
Nagwa E A Gaboon, Asia Parveen, Khaled A Ahmad, et al.
Journal of Molecular Neuroscience : MN
|
October 4, 2024
Clinical and Molecular Profiles of a Cohort of Egyptian Patients with Collagen VI-Related Dystrophy
Wessam E Sharaf-Eldin, Karima Rafat, Mahmoud Y Issa, et al.
Saudi Journal of Biological Sciences
|
January 1, 2020
Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects
Nagwa E A Gaboon, Babajan Banaganapalli, Khalidah Nasser, et al.
Page
of 1