Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis by Wilkie, Andrew O M, Byren, Jo C, Hurst, Jane A, Jayamohan, Jayaratnam, Johnson, David, Knight, Samantha J L, Lester, Tracy, Richards, Peter G, Twigg, Stephen R F, Wall, Steven A

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A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis by 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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Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits by Nicoletti, Paola, Zafer, Samreen, Matok, Lital, Irron, Inbar, Patrick, Meidva, Haklai, Rotem, Evangelista, John Erol, Marino, Giacomo B., Ma’ayan, Avi, Sewda, Anshuman, Holmes, Greg, Britton, Sierra R., Lee, Won Jun, Wu, Meng, Ru, Ying, Arnaud, Eric, Botto, Lorenzo, Brody, Lawrence C., Byren, Jo C., Caggana, Michele, Carmichael, Suzan L., Cilliers, Deirdre, Conway, Kristin, Crawford, Karen, Cuellar, Araceli, Di Rocco, Federico, Engel, Michael, Fearon, Jeffrey, Feldkamp, Marcia L., Finnell, Richard, Fisher, Sarah, Freudlsperger, Christian, Garcia-Fructuoso, Gemma, Hagge, Rhinda, Heuzé, Yann, Harshbarger, Raymond J., Hobbs, Charlotte, Howley, Meredith, Jenkins, Mary M., Johnson, David, Justice, Cristina M., Kane, Alex, Kay, Denise, Gosain, Arun Kumar, Langlois, Peter, Legal-Mallet, Laurence, Lin, Angela E., Mills, James L., Morton, Jenny E.V., Noons, Peter, Olshan, Andrew, Persing, John, Phipps, Julie M., Redett, Richard, Reefhuis, Jennita, Rizk, Elias, Samson, Thomas D., Shaw, Gary M., Sicko, Robert, Smith, Nataliya, Staffenberg, David, Stoler, Joan, Sweeney, Elizabeth, Taub, Peter J., Timberlake, Andrew T., Topczewska, Jolanta, Wall, Steven A., Wilson, Alexander F., Wilson, Louise C., Boyadjiev, Simeon A., Wilkie, Andrew O.M., Richtsmeier, Joan T., Jabs, Ethylin Wang, Romitti, Paul A., Karasik, David, Birnbaum, Ramon Y., Peter, Inga

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Etiological heterogeneity and clinical characteristics of metopic synostosis: Evidence from a tertiary craniofacial unit by Kini, Usha, Hurst, Jane A., Byren, Jo C., Wall, Steven A., Johnson, David, Wilkie, Andrew O.M.

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Clinical dividends from the molecular genetic diagnosis of craniosynostosis by Wilkie, Andrew O.M., Bochukova, Elena G., Hansen, Ruth M. S., Taylor, Indira B., Rannan-Eliya, Sahan V., Byren, Jo C., Wall, Steven A., Ramos, Lina, Venâncio, Margarida, Hurst, Jane A., O'Rourke, Anthony W., Williams, Louise J., Seller, Anneke, Lester, Tracy

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Clinical dividends from the molecular genetic diagnosis of craniosynostosis by Wilkie, Andrew O.M., Bochukova, Elena G., Hansen, Ruth M. S., Taylor, Indira B., Rannan-Eliya, Sahan V., Byren, Jo C., Wall, Steven A., Ramos, Lina, Venâncio, Margarida, Hurst, Jane A., O'Rourke, Anthony W., Williams, Louise J., Seller, Anneke, Lester, Tracy

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