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International Journal of Molecular Sciences
|
January 8, 2025
Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman
Vijay Gupta, Afif Ben-Mahmoud, Ahmed B Idris, et al.
Sultan Qaboos University Medical Journal
|
June 9, 2015
Incidence and Risk Factors of Parenteral Nutrition-Associated Cholestasis in Omani Neonates: Single centre experience
Sharef W Sharef, Siham Al-Sinani, Khalid Al-Naamani, et al.
Sultan Qaboos University Medical Journal
|
September 15, 2021
Intellectual Profile of Children with Autism Spectrum Disorder: Identification of verbal and nonverbal subscales predicting intelligence quotient
Watfa Al-Mamari, Ahmed B Idris, Ahlam Gabr, et al.
Orphanet Journal of Rare Diseases
|
November 4, 2023
Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families
Marwa Al Busaidi, Feda E Mohamed, Eiman Al-Ajmi, et al.
American Journal of Medical Genetics. Part A
|
May 6, 2016
Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family
Ahmed Al-Amri, Abeer Al Saegh, Watfa Al-Mamari, et al.
Clinical Genetics
|
August 21, 2018
Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits
Maryam Al-Nabhani, Samiya Al-Rashdi, Fathiya Al-Murshedi, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2022
Further phenotypic delineation of Alazami syndrome
Abdulhamid Al-Hinai, Samiya Al-Hashmi, Anuradha Ganesh, et al.
Global Public Health
|
July 25, 2024
Perception about telemedicine services among parents of children with neurodevelopmental disorders in a specialised tertiary centre in Oman
Ahmed B Idris, Watfa Al-Mamari, Taif Saud Al Humaidi, et al.
Journal of Autism and Developmental Disorders
|
February 28, 2025
Could a National Screening Program Reduce the Age of Diagnosis of Autism Spectrum Disorder?
Watfa Al-Mamari, Ahmed B Idris, Hafsa Al Aamri, et al.
International Journal of Developmental Disabilities
|
April 7, 2023
Applying whole exome sequencing in a consanguineous population with autism spectrum disorder
Watfa Al-Mamari, Ahmed B Idris, Khalid Al-Thihli, et al.
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Showing results (11-20 of 24) with videos related to
Sort By:
Page
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International Journal of Molecular Sciences
|
January 8, 2025
Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman
Vijay Gupta, Afif Ben-Mahmoud, Ahmed B Idris, et al.
Sultan Qaboos University Medical Journal
|
June 9, 2015
Incidence and Risk Factors of Parenteral Nutrition-Associated Cholestasis in Omani Neonates: Single centre experience
Sharef W Sharef, Siham Al-Sinani, Khalid Al-Naamani, et al.
Sultan Qaboos University Medical Journal
|
September 15, 2021
Intellectual Profile of Children with Autism Spectrum Disorder: Identification of verbal and nonverbal subscales predicting intelligence quotient
Watfa Al-Mamari, Ahmed B Idris, Ahlam Gabr, et al.
Orphanet Journal of Rare Diseases
|
November 4, 2023
Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families
Marwa Al Busaidi, Feda E Mohamed, Eiman Al-Ajmi, et al.
American Journal of Medical Genetics. Part A
|
May 6, 2016
Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family
Ahmed Al-Amri, Abeer Al Saegh, Watfa Al-Mamari, et al.
Clinical Genetics
|
August 21, 2018
Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits
Maryam Al-Nabhani, Samiya Al-Rashdi, Fathiya Al-Murshedi, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2022
Further phenotypic delineation of Alazami syndrome
Abdulhamid Al-Hinai, Samiya Al-Hashmi, Anuradha Ganesh, et al.
Global Public Health
|
July 25, 2024
Perception about telemedicine services among parents of children with neurodevelopmental disorders in a specialised tertiary centre in Oman
Ahmed B Idris, Watfa Al-Mamari, Taif Saud Al Humaidi, et al.
Journal of Autism and Developmental Disorders
|
February 28, 2025
Could a National Screening Program Reduce the Age of Diagnosis of Autism Spectrum Disorder?
Watfa Al-Mamari, Ahmed B Idris, Hafsa Al Aamri, et al.
International Journal of Developmental Disabilities
|
April 7, 2023
Applying whole exome sequencing in a consanguineous population with autism spectrum disorder
Watfa Al-Mamari, Ahmed B Idris, Khalid Al-Thihli, et al.
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of 3