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Author/Creator Naseer, Muhammad Imran

4. Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia. Issue 12 (9th December 2021)

Authors:
Alharazy, Shatha; Robertson, M Denise; Lanham-New, Susan; Naseer, Muhammad Imran; Chaudhary, Adeel G; Alissa, Eman
Journal:
Endocrine connections
Issue:
Volume 10:Issue 12(2022)
Page Start:
1594
Record Type:
Journal Article
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6. Microcephaly‐capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing. Issue 11 (17th August 2016)

Authors:
Naseer, Muhammad Imran; Sogaty, Sameera; Rasool, Mahmood; Chaudhary, Adeel G.; Abutalib, Yousif Ahmed; Walker, Susan; Marshall, Christian R.; Merico, Daniele; Carter, Melissa T.; Scherer, Stephen W.; Al‐Qahtani, Mohammad H.; Zarrei, Mehdi
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 11(2016)
Page Start:
3018
Record Type:
Journal Article
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7. Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. (27th October 2020)

Authors:
Khan, Muhammad Ismail; Latif, Muhammad; Saif, Maria; Ahmad, Hilal; Khan, Atta Ullah; Naseer, Muhammad Imran; Hussain, Hafiz Muhammad Jafar; Jelani, Musharraf
Journal:
Journal of gene medicine
Issue:
Volume 23:Number 1(2021)
Page Start:
n/a
Record Type:
Journal Article
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8. Whole exome sequencing identifies a novel compound heterozygous GFM1 variant underlying developmental delay, dystonia, polymicrogyria, and severe intellectual disability in a Pakhtun family. Issue 9 (15th June 2022)

Authors:
Khan, Atta Ullah; Khan, Ibrar; Khan, Muhammad Ismail; Latif, Muhammad; Siddiqui, Muhammad Imran; Khan, Shafi Ullah; Htar, Thet Thet; Wahid, Ghazala; Ullah, Ikram; Bibi, Fehmida; Khan, Asifullah; Naseer, Muhammad Imran; Seo, Go Hun; Jelani, Musharraf
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 9(2022)
Page Start:
2693
Record Type:
Journal Article
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