Watfa Al-Mamari - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Watfa Al-Mamari

Showing results (21-30 of 24) with videos related to

Pageof 3

Sort By:

You have reached the last page of results.This site can display upto 24 results.

European Journal of Medical Genetics|November 27, 2018

LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing lossAhmed H Al-Amri, Abeer Al Saegh, Watfa Al-Mamari, et al.

Sultan Qaboos University Medical Journal|July 11, 2025

Nurturing the Future: <i>Understanding maternal knowledge of child development in Oman</i>Watfa Al-Mamari, Ahmed B Idris, Saquib Jalees, et al.

Scientific Reports|November 7, 2022

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern familiesGhalia Al-Kasbi, Fathiya Al-Murshedi, Adila Al-Kindi, et al.

American Journal of Human Genetics|February 23, 2022

THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorderMartin Broly, Bogdan V Polevoda, Kamel M Awayda, et al.

Pageof 3

Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

European Journal of Medical Genetics|November 27, 2018

LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing lossAhmed H Al-Amri, Abeer Al Saegh, Watfa Al-Mamari, et al.

Sultan Qaboos University Medical Journal|July 11, 2025

Nurturing the Future: <i>Understanding maternal knowledge of child development in Oman</i>Watfa Al-Mamari, Ahmed B Idris, Saquib Jalees, et al.

Scientific Reports|November 7, 2022

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern familiesGhalia Al-Kasbi, Fathiya Al-Murshedi, Adila Al-Kindi, et al.

American Journal of Human Genetics|February 23, 2022

THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorderMartin Broly, Bogdan V Polevoda, Kamel M Awayda, et al.

Pageof 3