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American Journal of Hematology|August 30, 2016
Investigation of chromosome X inactivation and clinical phenotypes in female carriers of DKC1 mutationsJialin Xu, Payal P Khincha, Neelam Giri, et al.
Transplantation|March 1, 1988
A DNA-RFLP typing system that positively identifies serologically well-defined and ill-defined HLA-DR and DQ alleles, including DRw10J L Bidwell, E A Bidwell, D A Savage, et al.
British Journal of Haematology|July 1, 1995
Detection of beta-thalassaemia mutations using DNA heteroduplex generator moleculesD A Savage, N A Wood, J L Bidwell, et al.
Human Pathology|March 1, 1980
Acute nonlymphocytic leukemia in patients receiving chemotherapy for nonmalignant diseasesK Sheibani, R M Bukowski, R R Tubbs, et al.
Blood Advances|June 2, 2018
Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenitaPayal P Khincha, Alison A Bertuch, Shahinaz M Gadalla, et al.
Genes and Immunity|November 9, 2002
The IL12B 3' untranslated region DNA polymorphism is not associated with early-onset type 1 diabetesR M McCormack, A P Maxwell, D J Carson, et al.
The Journal of Trauma and Acute Care Surgery|February 23, 2022
Variations in clot phenotype following injury: The MA-R ratio and fragile clotsJames Harrington, Ben L Zarzaur, Erin E Fox, et al.
AJR. American Journal of Roentgenology|January 1, 1995
Percutaneous biopsy of the liver and kidney by using coaxial technique: adequacy of the specimen obtained with three different needles in vitroK D Hopper, R T Grenko, T R TenHave, et al.
ERJ Open Research|November 23, 2019
Prognostic significance of pulmonary function tests in dyskeratosis congenita, a telomere biology disorderNeelam Giri, Sandhiya Ravichandran, Youjin Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 10, 2004
Role of alpha-adducin DNA polymorphisms in the genetic predisposition to diabetic nephropathyBryan R Conway, Rosalind Martin, Amy-Jayne McKnight, et al.
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