Sensory substitution using tactile pin arrays : Human factors, technology and applications : Multimodal human-computer interfacesWALL, Steven A; BREWSTER, Stephen.Signal processing. 2006, Vol 86, Num 12, pp 3674-3695, issn 0165-1684, 22 p.Article

A high bandwidth interface for haptic human computer interactionWALL, Steven A; HARWIN, William.Mechatronics (Oxford). 2001, Vol 11, Num 4, pp 371-387, issn 0957-4158Article

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosisMERRILL, Amy E; BOCHUKOVA, Elena G; BRUGGER, Sean M et al.Human molecular genetics (Print). 2006, Vol 15, Num 8, pp 1319-1328, issn 0964-6906, 10 p.Article

Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary TeethNIEMINEN, Pekka; MORGAN, Neil V; BRUETON, Louise A et al.American journal of human genetics. 2011, Vol 89, Num 1, pp 67-81, issn 0002-9297, 15 p.Article

RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesityJENKINS, Dagan; SEELOW, Dominik; ØRSTAVIK, Karen Helene et al.American journal of human genetics. 2007, Vol 80, Num 6, pp 1162-1170, issn 0002-9297, 9 p.Article

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9JUSTICE, Cristina M; YAGNIK, Garima; KIMONIS, Virginia et al.Nature genetics. 2012, Vol 44, Num 12, pp 1360-1364, issn 1061-4036, 5 p.Article

Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patientsSARQUIS JEHEE, Fernanda; ALONSO, Luis G; PASSOS-BUENO, Maria Rita et al.The Cleft palate-craniofacial journal. 2006, Vol 43, Num 2, pp 148-151, issn 1055-6656, 4 p.Article

Monozygotic twins discordant for frontonasal malformationMOHAMMED, Shehla N; SWAN, Marc C; WALL, Steven A et al.American journal of medical genetics. 2004, Vol 130A, Num 4, pp 384-388, issn 0148-7299, 5 p.Article

Paternal origin of FGFR3 mutations in Muenke-type craniosynostosisRANNAN-ELIYA, Sahan V; TAYLOR, Indira B; DE HEER, I. Marieke et al.Human genetics. 2004, Vol 115, Num 3, pp 200-207, issn 0340-6717, 8 p.Article

Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosisKAN, Shih-Hsin; ELANKO, Navaratnam; MCDONALD-MCGINN, Donna M et al.American journal of human genetics. 2002, Vol 70, Num 2, pp 472-486, issn 0002-9297Article

Reoperation for Intracranial Hypertension in TWIST1-Confirmed Saethre-Chotzen Syndrome: A 15-Year Review. CommentaryWOODS, Roger H; UL-HAQ, Ehtesham; WILKIE, Andrew O. M et al.Plastic and reconstructive surgery (1963). 2009, Vol 123, Num 6, pp 1801-1812, issn 0032-1052, 12 p.Article

Clinical dividends from the molecular genetic diagnosis of craniosynostosisWILKIE, Andrew O. M; BOCHUKOVA, Elena G; O'ROURKE, Anthony W et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 16, pp 1941-1949, issn 1552-4825, 9 p.Article

The origin of EFNB1 mutations in craniofrontonasal syndrome : Frequent somatic mosaicism and explanation of the paucity of carrier malesTWIGG, Stephen R. F; MATSUMOTO, Kazuya; SWEENEY, Elizabeth et al.American journal of human genetics. 2006, Vol 78, Num 6, pp 999-1010, issn 0002-9297, 12 p.Article

Fibroblast growth factor receptor 2, gain-of-function mutations, and tumourigenesis : investigating a potential linkHANSEN, Ruth M. S; GORIELY, Anne; WALL, Steven A et al.Journal of pathology. 2005, Vol 207, Num 1, pp 27-31, issn 0022-3417, 5 p.Article

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defectsMAVROGIANNIS, Lampros A; ANTONOPOULOU, Ileana; BAXOVA, Alica et al.Nature genetics. 2001, Vol 27, Num 1, pp 17-18, issn 1061-4036Article

Interaction of visual and haptic information in simulated environments: Texture perceptionWALL, Steven A; HARWIN, William S.Lecture notes in computer science. 2001, pp 108-117, issn 0302-9743, isbn 3-540-42356-7Conference Paper

Atypical Crouzon Syndrome With a Novel Cys62Arg Mutation in FGFR2 Presenting With Sagittal SynostosisSHARMA, Vikram P; WALL, Steven A; LORD, Helen et al.The Cleft palate-craniofacial journal. 2012, Vol 49, Num 3, pp 373-377, issn 1055-6656, 5 p.Article

Etiological Heterogeneity and Clinical Characteristics of Metopic Synostosis: Evidence From a Tertiary Craniofacial UnitKINI, Usha; HURST, Jane A; BYREN, Jo C et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 6, pp 1383-1389, issn 1552-4825, 7 p.Article

Scalp fibroblasts have a shared expression profile in monogenic craniosynostosisBOCHUKOVA, Elena G; SONEJI, Shamit; WALL, Steven A et al.Journal of medical genetics. 2010, Vol 47, Num 12, pp 803-808, issn 0022-2593, 6 p.Article

Hearing loss in a mouse model of Muenke syndromeMANSOUR, Suzanne L; TWIGG, Stephen R. F; FREELAND, Rowena M et al.Human molecular genetics (Print). 2009, Vol 18, Num 1, pp 43-50, issn 0964-6906, 8 p.Article

Implications of a Vertex Bulge following Modified Strip Craniectomy for Sagittal SynostosisMARUCCI, Damian D; JOHNSTON, Christine P; ANSLOW, Philip et al.Plastic and reconstructive surgery (1963). 2008, Vol 122, Num 1, pp 217-224, issn 0032-1052, 8 p.Article

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