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Journal of Medical Genetics|August 3, 2000
Detailed mapping of a congenital heart disease gene in chromosome 3p25E K Green, M D Priestley, J Waters, et al.
Molecular Pathology : MP|July 18, 2000
Role of chromosome 3p12-p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesisA Martinez, P Fullwood, K Kondo, et al.
Human Mutation|October 7, 2006
Genotype-phenotype correlations in von Hippel-Lindau diseaseKai Ren Ong, Emma R Woodward, Pip Killick, et al.
Cancer Research|January 20, 2007
Depletion of the Ras association domain family 1, isoform A-associated novel microtubule-associated protein, C19ORF5/MAP1S, causes mitotic abnormalitiesAshraf Dallol, Wendy N Cooper, Fahd Al-Mulla, et al.
Dalton Transactions (Cambridge, England : 2003)|April 18, 2012
Diisocyanoarene-linked pentacarbonylvanadate(I-) ions as building blocks in a supramolecular charge-transfer framework assembled through noncovalent π-π and contact ion interactionsTiffany R Maher, John J Meyers, Andrew D Spaeth, et al.
Clinical Nephrology|March 1, 1989
Atherosclerotic renovascular disease causing renal impairment--a case for treatmentJ E Scoble, E R Maher, G Hamilton, et al.
Molecular Pathology : MP|May 29, 2002
Mutation screening analysis of the retinoblastoma related gene RB2/p130 in sporadic ovarian cancer and head and neck squamous cell cancerA J Alvi, R Hogg, J S Rader, et al.
Endocrine|August 17, 2013
Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidismHakan Cangul, Kristien Boelaert, Murat Dogan, et al.
Clinical Genetics|February 25, 2020
A recurrent pathogenic variant in TPM2 reveals further phenotypic and genetic heterogeneity in multiple pterygium syndrome-related disordersJulie Vogt, Atif Al-Saedi, Tracey Willis, et al.
Epigenetics|February 23, 2013
DNA methylation profiling distinguishes histological subtypes of renal cell carcinomaAmy A Slater, Majed Alokail, Dean Gentle, et al.
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