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Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.
Nat Genet. 2002 May;31(1):79-83. doi: 10.1038/ng874. Epub 2002 Apr 8.
Nat Genet. 2002.
PMID: 11941370
Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes.
Hearn T, Spalluto C, Phillips VJ, Renforth GL, Copin N, Hanley NA, Wilson DI.
Hearn T, et al. Among authors: renforth gl.
Diabetes. 2005 May;54(5):1581-7. doi: 10.2337/diabetes.54.5.1581.
Diabetes. 2005.
PMID: 15855349
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Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis.
Phillips HM, Renforth GL, Spalluto C, Hearn T, Curtis AR, Craven L, Havarani B, Clement-Jones M, English C, Stumper O, Salmon T, Hutchinson S, Jackson MS, Wilson DI.
Phillips HM, et al. Among authors: renforth gl.
Genomics. 2002 Apr;79(4):475-8. doi: 10.1006/geno.2002.6742.
Genomics. 2002.
PMID: 11944976
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Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings.
Cox H, Lucassen A, Rio M, Browne C, Renforth G, Craven L, Salmon T, Wilson DI.
Cox H, et al.
Clin Dysmorphol. 2009 Apr;18(2):98-102. doi: 10.1097/MCD.0b013e3283202a1f.
Clin Dysmorphol. 2009.
PMID: 19077675
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Endoglin, an ancillary TGFbeta receptor, is required for extraembryonic angiogenesis and plays a key role in heart development.
Arthur HM, Ure J, Smith AJ, Renforth G, Wilson DI, Torsney E, Charlton R, Parums DV, Jowett T, Marchuk DA, Burn J, Diamond AG.
Arthur HM, et al.
Dev Biol. 2000 Jan 1;217(1):42-53. doi: 10.1006/dbio.1999.9534.
Dev Biol. 2000.
PMID: 10625534
Free article.
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