Arama Sonuçları - Salman Kirmani
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Compound heterozygosity for a whole gene deletion and p.R124C mutation in causing nonclassic congenital adrenal hyperplasia Yazar: Hamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman Kirmani
Baskı/Yayın Bilgisi 2018Yer Numarası: Yüklüyor…Connect to this object online.
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2
Experience in prenatal genetic testing and reproductive decision-making for monogenic disorders from a single tertiary care genetics clinic in a low-middle income country Yazar: Amna Hanif, Fizza Akbar, Salman Kirmani, Amyna Jaffarali, Ghulam Zainab, Ayesha Malik, Zeeshan Ansar, Bushra Afroze
Baskı/Yayın Bilgisi 2023Yer Numarası: Yüklüyor…Connect to this object online.
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3
Factors associated with changes in the quality of life and family functioning scores of primary caregivers of children and young people with primary brain tumors in Karachi, Pakist... Yazar: Nida Zahid, Syed Ather Enam, Thomas Mårtensson, Iqbal Azam, Naureen Mushtaq, Mariya Moochhala, Faiza Kausar, Aneesa Hassan, Saqib Kamran Bakhshi, Farrukh Javed, Lal Rehman, Muhammad Nouman Mughal, Sadaf Altaf, Salman Kirmani, Nick Brown
Baskı/Yayın Bilgisi 2024Yer Numarası: Yüklüyor…Connect to this object online.
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