Citation: K. Becker et M. Splitt, A family with distal arthrogryposis and cleft palate: possible overlap between Gordon syndrome and Aase-Smith syndrome, CLIN DYSMOR, 10(1), 2001, pp. 41-45
Authors:
de Vries, BBA
White, SM
Knight, SJL
Regan, R
Homfray, T
Young, ID
Super, M
McKeown, C
Splitt, M
Quarrell, OWJ
Trainer, AH
Niermeijer, MF
Malcolm, S
Flint, J
Hurst, JA
Winter, RM
Citation: Bba. De Vries et al., Clinical studies on submicroscopic subtelomeric rearrangements: a checklist, J MED GENET, 38(3), 2001, pp. 145-150
Authors:
Bamford, RN
Roessler, E
Burdine, RD
Saplakoglu, U
dela Cruz, J
Splitt, M
Goodship, JA
Towbin, J
Bowers, P
Ferrero, GB
Marino, B
Schier, AF
Shen, MM
Muenke, M
Casey, B
Citation: Rn. Bamford et al., Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects (vol 26, pg 365, 2000), NAT GENET, 26(4), 2000, pp. 501-501
Authors:
Bamford, RN
Roessler, E
Burdine, RD
Saplakoglu, U
dela Cruz, J
Splitt, M
Towbin, J
Bowers, P
Marino, B
Schier, AF
Shen, MM
Muenke, M
Casey, B
Citation: Rn. Bamford et al., Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects, NAT GENET, 26(3), 2000, pp. 365-369
Authors:
Tassabehji, M
Metcalfe, K
Karmiloff-Smith, A
Carette, MJ
Grant, J
Dennis, N
Reardon, W
Splitt, M
Read, AP
Donnai, D
Citation: M. Tassabehji et al., Williams syndrome: Use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes, AM J HU GEN, 64(1), 1999, pp. 118-125