Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Craniosynostosis[original query] |
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A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
Nature genetics 2012 Nov . Justice CM, Yagnik G, Kim Y, Peter I, Jabs EW, Erazo M, Ye X, Ainehsazan E, Shi L, Cunningham ML, Kimonis V, Roscioli T, Wall SA, Wilkie AO, Stoler J, Richtsmeier JT, Heuzé Y, Sanchez-Lara PA, Buckley MF, Druschel CM, Mills JL, Caggana M, Romitti PA, Kay DM, Senders C, Taub PJ, Klein OD, Boggan J, Zwienenberg-Lee M, Naydenov C, Kim J, Wilson AF, Boyadjiev SA |
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Human genetics 2020 Apr . Justice Cristina M, Cuellar Araceli, Bala Krithi, Sabourin Jeremy A, Cunningham Michael L, Crawford Karen, Phipps Julie M, Zhou Yan, Cilliers Deirdre, Byren Jo C, Johnson David, Wall Steven A, Morton Jenny E V, Noons Peter, Sweeney Elizabeth, Weber Astrid, Rees Katie E M, Wilson Louise C, Simeonov Emil, Kaneva Radka, Yaneva Nadezhda, Georgiev Kiril, Bussarsky Assen, Senders Craig, Zwienenberg Marike, Boggan James, Roscioli Tony, Tamburrini Gianpiero, Barba Marta, Conway Kristin, Sheffield Val C, Brody Lawrence, Mills James L, Kay Denise, Sicko Robert J, Langlois Peter H, Tittle Rachel K, Botto Lorenzo D, Jenkins Mary M, LaSalle Janine M, Lattanzi Wanda, Wilkie Andrew O M, Wilson Alexander F, Romitti Paul A, Boyadjiev Simeon A, |
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