J. Hamlington

发表

Deletion of a branch-point consensus sequence in the LMX1B gene causes exon skipping in a family with nail patella syndrome

J. Hamlington, M. Clough, J. A. Dunston, 2000, European Journal of Human Genetics.

Platelet Glycoprotein IIIa Pl A Polymorphism and Effects of Aspirin on Thrombin Generation

M. Furman, A. Michelson, P. Bray, 2001 .

PlA2 polymorphism and efficacy of aspirin

P. Bray, P. Goldschmidt-Clermont, G. Cooke, 1998, The Lancet.

Platelet GP IIIa Pl(A) polymorphisms display different sensitivities to agonists.

M. Furman, M. Mascelli, S. Kundu, 2000, Circulation.

Use of DNA Sequencing Analysis To Confirm Fungemia Due to Trichosporon dermatis in a Pediatric Patient

S. Gunn, T. Johnson-Pais, J. Jorgensen, 2006, Journal of Clinical Microbiology.

A complex population of RNAs exists in human ejaculate spermatozoa: implications for understanding molecular aspects of spermiogenesis.

S. Rollinson, R. Lilford, H. Snowden, 1999, Gene.

Prenatal detection of rhesus D genotype

G. Mason, J. Hamlington, J. Cunningham, 1997, The Lancet.

A single nucleotide polymorphism in MGEA5 encoding O-GlcNAc-selective N-acetyl-beta-D glucosaminidase is associated with type 2 diabetes in Mexican Americans.

R. Duggirala, J. Blangero, T. Dyer, 2005, Diabetes.

Restricted distribution of loss‐of‐function mutations within the LMX1B genes of nail‐patella syndrome patients

J. Hamlington, M. Clough, I. Mcintosh, 1999, Human mutation.

A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American family

R. Duggirala, J. Blangero, K. Hunt, 2006, Diabetes/metabolism research and reviews.

The human LMX1B gene: transcription unit, promoter, and pathogenic mutations.

R. Mountford, E. Sweeney, J. Sibbring, 2004, Genomics.

Evaluation of Tight Junction Protein 1 Encoding Zona Occludens 1 as a Candidate Gene for Albuminuria in a Mexican American Population

L. Almasy, R. Duggirala, H. Abboud, 2006, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Haplotypes of Transcription Factor 7–Like 2 (TCF7L2) Gene and Its Upstream Region Are Associated With Type 2 Diabetes and Age of Onset in Mexican Americans

R. Duggirala, J. Blangero, K. Hunt, 2007, Diabetes.

Twenty‐two novel LMX1B mutations identified in nail patella syndrome (NPS) patients

J. Hamlington, I. Mcintosh, Cheron Jones, 2001, Human mutation.

Non‐invasive RNA‐based determination of fetal Rhesus D type: a prospective study based on 96 pregnancies

G. Mason, J. Hamlington, J. Cunningham, 1999, British journal of obstetrics and gynaecology.