First Report of a Derivative Chromosome 13 with a Duplicated 11p15 Locus Associated with Silver-Russell Syndrome

por Hamza, Nishath, Al-Araimi, Musallam, Al Salmani, Kamla, Al Obeidani, Salwa
Publicado 2023

A first case report of hypohidrotic ectodermal dysplasia from Oman

por Al‐Araimi, Musallam, Hamza, Nishath, Al Hosni, Aliya, Al Mazrooey, Hiba
Publicado 2020

Hereditary Paraganglioma in an Omani Family

por Pambinezhthu, Fathima, Hamza, Nishath, Al Kharusi, Manal, Ramadhan, Fatma, Al Busaidi, Noor, Kamona, Atheel
Publicado 2021

A Novel SPINK5 Gene Mutation Associated with Netherton Syndrome in an Omani Patient

por Hamza, Nishath, Al Sukaiti, Nashat, Ahmed, Khwater A.M., Romano, Rosa, Gokhale, Uday A., Pan-Hammarström, Qiang
Publicado 2021

Rare NF1 microdeletion syndrome in an Omani patient

por Al‐Araimi, Musallam, Hamza, Nishath, Al Yahmadi, Ali, Al Mazrooey, Hiba, Elsheikh, Afaf, Al Amri, Amira, Al Harrasi, Salma, Hausdorf, Lena, Mula‐Abed, Waad‐Allah
Publicado 2018

Repository of mutations from Oman: The entry point to a national mutation database

por Rajab, Anna, Hamza, Nishath, Al Harasi, Salma, Al Lawati, Fatma, Gibbons, Una, Al Alawi, Intesar, Kobus, Karoline, Hassan, Suha, Mahir, Ghariba, Al Salmi, Qasim, Mons, Barend, Robinson, Peter
Publicado 2015