Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene. by Boultwood, J, Strickson, A, Jabs, E, Cheng, J, Fidler, C, Wainscoat, J

ISOLATION OF NOVEL CDNA CLONES MAPPING TO THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME by Boultwood, J, Fidler, C, Jabs, E, Lovett, M, Hedge, P, Markham, A, Cotter, F, Wainscoat, J

Isolation and analysis of novel candidate genes mapping to the critical region of the 5q-syndrome. by Boultwood, J, Fidler, C, Strickson, A, Watkins, F, Kostrzewa, M, Jaju, R, Muller, U, Jabs, E, Cheng, J, Wainscoat, J

Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. by Jehee, F, Alonso, L, Cavalcanti, D, Kim, C, Wall, SA, Mulliken, J, Sun, M, Jabs, E, Boyadjiev, SA, Wilkie, A, Passos-Bueno, MR

Primary transcription map of the critical region of the 5q-syndrome. by Boultwood, J, Fidler, C, Soularue, P, Kostrzewa, M, Strickson, A, Jaju, R, Cotter, F, Jabs, E, Lovett, M, Muller, U, Auffray, C, Wainscoat, W

Isolation and analysis of novel genes mapping to the critical region of the 5q-syndrome by Fidler, C, Strickson, A, Soularue, P, Kostrzewa, M, Jaju, R, Watkins, F, Monaco, A, Muller, U, Lovett, M, Jabs, E, Auffray, C, Boultwood, J, Wainscoat, J

Novel genes mapping to the critical region of the 5q- syndrome. by Boultwood, J, Fidler, C, Soularue, P, Strickson, A, Kostrzewa, M, Jaju, R, Cotter, F, Fairweather, N, Monaco, A, Müller, U, Lovett, M, Jabs, E, Auffray, C, Wainscoat, J

Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. by Jehee, F, Johnson, D, Alonso, L, Cavalcanti, D, de Sá Moreira, E, Alberto, F, Kok, F, Kim, C, Wall, SA, Jabs, E, Boyadjiev, SA, Wilkie, A, Passos-Bueno, MR

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9 by Justice, C, Yagnik, G, Kim, Y, Peter, I, Jabs, E, Erazo, M, Ye, X, Ainehsazan, E, Shi, L, Cunningham, M, Kimonis, V, Roscioli, T, Wall, SA, Wilkie, A, Stoler, J, Richtsmeier, J, Heuzé, Y, Sanchez-Lara, P, Buckley, M, Druschel, C, Mills, J, Caggana, M, Romitti, P, Kay, D, Senders, C

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. by Justice, C, Yagnik, G, Kim, Y, Peter, I, Jabs, E, Erazo, M, Ye, X, Ainehsazan, E, Shi, L, Cunningham, M, Kimonis, V, Roscioli, T, Wall, SA, Wilkie, A, Stoler, J, Richtsmeier, J, Heuzé, Y, Sanchez-Lara, P, Buckley, M, Druschel, C, Mills, J, Caggana, M, Romitti, P, Kay, D, Senders, C