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:
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:
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:
Smith, SJ
Rucka, AK
Berry, JL
Davies, M
Mylchreest, S
Paterson, CR
Heath, DA
Tassabehji, M
Read, AP
Mee, AP
Mawer, EB
Citation: Sj. Smith et al., Novel mutations in the 1 alpha-hydroxylase (P450cl) gene in three familieswith pseudovitamin D-deficiency rickets resulting in loss of functional enzyme activity in blood-derived macrophages, J BONE MIN, 14(5), 1999, pp. 730-739
Authors:
Tassabehji, M
Romer, U
Hauswald, B
Huttenbrink, KB
Citation: M. Tassabehji et al., Determination of provocation threshold of the nasal provocation test (NPT)in patients with allergic rhinitis, ALLERGOLOGI, 22(7), 1999, pp. 404-410
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