Author/Creator: Naeemi, Humaira - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Naeemi, Humaira

1. A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome. Issue 1 (December 2016)

Authors:: Rashid, Muhammad; Naeemi, Humaira; Muhammad, Noor; Loya, Asif; Yusuf, Muhammed; Lubiński, Jan; Jakubowska, Anna; Hamann, Ute
Journal:: Hereditary cancer in clinical practice
Issue:: Volume 14:Issue 1(2016)
Page Start:: 1
Record Type:: Journal Article
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2. Absence of the TRIP13 c.1060C>T Mutation in Wilms Tumor Patients From Pakistan. Issue 3 (April 2020)

Authors:: Rashid, Muhammad U.; Naeemi, Humaira; Qazi, Abid Q.; Muhammad, Noor; Ahmad, Mansoor; Akhtar, Noreen; Rahman, Nazneen
Journal:: Journal of pediatric hematology/oncology
Issue:: Volume 42:Issue 3(2020)
Page Start:
Record Type:: Journal Article
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3. Chasing the origin of 23 recurrent BRCA1 mutations in Pakistani breast and ovarian cancer patients. Issue 3 (12th April 2022)

Authors:: Rashid, Muhammad Usman; Muhammad, Noor; Naeemi, Humaira; Shehzad, Umara; Hamann, Ute
Journal:: International journal of cancer
Issue:: Volume 151:Issue 3(2022)
Page Start:: 402
Record Type:: Journal Article
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4. Contribution of germline PALB2 variants to an unselected and prospectively registered pancreatic cancer patient cohort in Pakistan. Issue 12 (December 2022)

Authors:: Muhammad, Noor; Sadaqat, Rida; Naeemi, Humaira; Masood, Iqra; Hassan, Usman; Ijaz, Bushra; Hanif, Faisal; Syed, Aamir A.; Yusuf, Muhammed A.; Rashid, Muhammad U.
Journal:: HPB
Issue:: Volume 24:Issue 12(2022)
Page Start:: 2134
Record Type:: Journal Article
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