日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family

克什米尔近亲家族中一种复发性NECTIN4无义突变导致外胚层发育不良-并指综合征,并伴有新的表型

Ali, Ghazanfar; Sadia, Sadia; Ain-Ul-Batool, Syeda; Azeem, Zahid; Awan, Naheed Bashir; Kazmi, Syed Akif Raza; Ur-Rehman, Zia-; Anjum, Zeeshan; Ur-Rehman, Fazal-; Wali, Abdul; Khan, Kafaitullah; Zaman, Nasib; Ayub, Muhammad; Sajid, Muhammad; Hassan, Noor

Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome

在克什米尔一个患有巴德-比德尔综合征的家族中鉴定出BBS2基因中的一种新的纯合错义突变(c.443A>T:p.N148I)

Ali, Ghazanfar; Sadia; Foo, Jia Nee; Nasir, Abdul; Chang, Chu-Hua; Chew, Elaine GuoYan; Latif, Zahid; Azeem, Zahid; Ain-Ul-Batool, Syeda; Kazmi, Syed Akif Raza; Awan, Naheed Bashir; Khan, Abdul Hameed; Rehman, Fazal-Ur-; Khalid, Madiha; Wali, Abdul; Sarwar, Samina; Akhtar, Wasim; Ahmed Abbasi, Ansar; Nisar, Rameez

Sequencing and Characterization of Mitochondrial Protein-Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration

黑裂腹鱼(鲤形目:鲤科)线粒体蛋白编码基因的测序和表征及其系统发育意义

Akhtar, Tasleem; Ali, Ghazanfar; Shafi, Nuzhat; Akhtar, Wasim; Khan, Abdul Hameed; Latif, Zahid; Wali, Abdul; Ain-Ul-Batool, Syeda; Khan, Abdul Rehman; Mumtaz, Sadia; Altaf, Syed Iftikhar; Khawaja, Sundus; Sadia; Khalid, Madiha; Rehman, Fazal Ur; Javid, Qudir