A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA

od Walsh, Vanessa L., Raviv, Dorith, Dror, Amiel A., Shahin, Hashem, Walsh, Tom, Kanaan, Moien N., Avraham, Karen B., King, Mary-Claire
Izdano u Mamm Genome (2010)

Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

od Kamal, Lara, Pierce, Sarah B., Canavati, Christina, Rayyan, Amal Abu, Jaraysa, Tamara, Lobel, Orit, Lolas, Suhair, Norquist, Barbara M., Rabie, Grace, Zahdeh, Fouad, Levy-Lahad, Ephrat, King, Mary-Claire, Kanaan, Moien N.
Izdano u Cold Spring Harb Mol Case Stud (2020)

Genomic analysis of inherited hearing loss in the Palestinian population

od Abu Rayyan, Amal, Kamal, Lara, Casadei, Silvia, Brownstein, Zippora, Zahdeh, Fouad, Shahin, Hashem, Canavati, Christina, Dweik, Dima, Jaraysa, Tamara, Rabie, Grace, Carlson, Ryan J., Gulsuner, Suleyman, Lee, Ming K., Avraham, Karen B., Walsh, Tom, King, Mary-Claire, Kanaan, Moien N.
Izdano u Proc Natl Acad Sci U S A (2020)