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Author/Creator Irshad, Saba

1. An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan. Issue 9 (17th July 2020)

Authors:
Rasool, Sajida; Baig, Jamshaid Mahmood; Moawia, Abubakar; Ahmad, Ilyas; Iqbal, Maria; Waseem, Syeda Seema; Asif, Maria; Abdullah, Uzma; Makhdoom, Ehtisham Ul Haq; Kaygusuz, Emrah; Zakaria, Muhammad; Ramzan, Shafaq; Haque, Saif ul; Mir, Asif; Anjum, Iram; Fiaz, Mehak; Ali, Zafar; Tariq, Muhammad; ...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 9(2020)
Page Start:
n/a
Record Type:
Journal Article
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3. Mutations of KIF14 cause primary microcephaly by impairing cytokinesis. Issue 4 (14th October 2017)

Authors:
Moawia, Abubakar; Shaheen, Ranad; Rasool, Sajida; Waseem, Syeda Seema; Ewida, Nour; Budde, Birgit; Kawalia, Amit; Motameny, Susanne; Khan, Kamal; Fatima, Ambrin; Jameel, Muhammad; Ullah, Farid; Akram, Talia; Ali, Zafar; Abdullah, Uzma; Irshad, Saba; Höhne, Wolfgang; Noegel, Angelika Anna; Al‐Owai...
Journal:
Annals of neurology
Issue:
Volume 82:Issue 4(2017)
Page Start:
562
Record Type:
Journal Article
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4. Targeted gene sequencing of FYCO1 identified a novel mutation in a Pakistani family for autosomal recessive congenital cataract. Issue 8 (31st May 2022)

Authors:
Saleem, Rani Saira; Siddiqui, Sorath Noorani; Irshad, Saba; Ashraf, Naeem Mahmood; Hamid, Arslan; Khan, Muhammad Azmat Ullah; Khan, Muhammad Imran; Micheal, Shazia
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 10:Issue 8(2022)
Page Start:
n/a
Record Type:
Journal Article
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