Full Text Journal Articles by
Author Noorjehan Sarfraz

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Frequency of FMR1 gene mutation and CGG repeat polymorphism in intellectually disabled children in Pakistan.

Tasneem Fatima, Syed Aley Hasan Zaidi, Noorjehan Sarfraz, Siddiqa Perween, Faraz Khurshid, Fauzia Imtiaz,

Fragile X syndrome is considered the most common heritable form of X-linked intellectual disability (ID). The syndrome is caused by silencing of the fragile X mental retardation 1 gene (Xq27.3) due to hypermethylation. This mutation results in absence or deficit of its protein product, the fragile X mental retardation protein ... Read more >>

Am J Med Genet A (American journal of medical genetics. Part A)
[2014, 164A(5):1151-1161]

Cited: 1 time

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Effect of chronic treatment with a cyclooxygenase inhibitor on reproductive parameters in male rat.

Sheikh A Saeed, Naheed Anwar, Khalid M Khan, Noorjehan Sarfraz,

BACKGROUND: Indomethacin is a member of non-steroidal anti-inflammatory drugs (NSAIDs) commonly used for treatment of gout, arthritis, and other inflammatory conditions. It has been shown to inhibit ovarian prostaglandins synthesis in mammals, birds, fish and reptiles. However, the effects of its chronic administration on male reproductive functions remain largely unknown. ... Read more >>

J Ayub Med Coll Abbottabad (Journal of Ayub Medical College, Abbottabad : JAMC)
[2009, 21(3):66-71]

Cited: 1 time

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