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2. A candidate transacting modulator of fetal hemoglobin gene expression in the Arab—Indian haplotype of sickle cell anemia. Issue 11 (22nd August 2016)

3. A rare missense variant of CASP7 is associated with familial late‐onset Alzheimer's disease. Issue 3 (29th November 2018)

4. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0‐thalassaemia homozygotes. (27th February 2017)

5. Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease. Issue 2 (20th June 2021)

7. Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia. Issue 6 (28th April 2016)

9. The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease. (14th September 2018)

10. The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes. (13th January 2016)