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Journal Article
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, ul Haque, Saif, Mir, Asif, Anjum, Iram 
ORCID: 0000-0002-9015-3179, Fiaz, Mehak, Ali, Zafar, Tariq, Muhammad, Saba, Neelam, Hussain, Wajid, Budde, Birgit, Irshad, Saba, Noegel, Angelika Anna, Hoening, Stefan, Baig, Shahid Mahmood, Nuernberg, Peter and Hussain, Muhammad Sajid
(2020).
An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.
Mol. Genet. Genom. Med., 8 (9).
HOBOKEN:
WILEY.
ISSN 2324-9269
Rasool, Sajida, Irshad, Saba, Saba, Neelam, Fiaz, Mehak, Hussain, Muhammad Sajid ORCID: 0000-0002-1353-8809, Hussain, Muhammad Wajid and Nuernberg, Peter
(2020).
A Novel Homozygous Nonsense Variant in BICD2 Underlies Hereditary Spastic Paraplegia Complex Type.
Pak. J. Zool., 52 (2).
S. 727 - 733.
LAHORE:
ZOOLOGICAL SOC PAKISTAN.
ISSN 0030-9923