Authors:
Metcalfe, K
Rucka, AK
Smoot, L
Hofstadler, G
Tuzler, G
McKeown, P
Siu, V
Rauch, A
Dean, J
Dennis, N
Ellis, I
Reardon, W
Cytrynbaum, C
Osborne, L
Yates, JR
Read, AP
Donnai, D
Tassabehji, M
Citation: K. Metcalfe et al., Elastin: mutational spectrum in supravalvular aortic stenosis, EUR J HUM G, 8(12), 2000, pp. 955-963
Authors:
Liede, A
Metcalfe, K
Hanna, D
Hoodfar, E
Snyder, C
Durham, C
Lynch, HT
Narod, SA
Citation: A. Liede et al., Evaluation of the needs of male carriers of mutations in BRCA1 or BRCA2 who have undergone genetic counseling, AM J HU GEN, 67(6), 2000, pp. 1494-1504
Authors:
Tassabehji, M
Carrette, M
Wilmot, C
Donnai, D
Read, AP
Metcalfe, K
Citation: M. Tassabehji et al., A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome, EUR J HUM G, 7(7), 1999, pp. 737-747
Authors:
Borsani, G
DeGrandi, A
Ballabio, A
Bulfone, A
Bernard, L
Banfi, S
Gattuso, C
Mariani, M
Dixon, M
Donnai, D
Metcalfe, K
Winter, R
Robertson, M
Axton, R
Brown, A
van Heyningen, V
Hanson, I
Citation: G. Borsani et al., EYA4, a novel vertebrate gene related to Drosophila eyes absent, HUM MOL GEN, 8(1), 1999, pp. 11-23
Authors:
Hockenhull, EL
Carette, MJ
Metcalfe, K
Donnai, D
Read, AP
Tassabehji, M
Citation: El. Hockenhull et al., A complete physical contig and partial transcript map of the Williams syndrome critical region, GENOMICS, 58(2), 1999, pp. 138-145
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