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A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. [electronic resource] by
- Johnson, D
- Horsley, S W
- Moloney, D M
- Oldridge, M
- Twigg, S R
- Walsh, S
- Barrow, M
- Njølstad, P R
- Kunz, J
- Ashworth, G J
- Wall, S A
- Kearney, L
- Wilkie, A O
Producer: 19981223
In:
American journal of human genetics vol. 63
Availability: No items available.
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Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2. [electronic resource] by
- Oldridge, M
- Lunt, P W
- Zackai, E H
- McDonald-McGinn, D M
- Muenke, M
- Moloney, D M
- Twigg, S R
- Heath, J K
- Howard, T D
- Hoganson, G
- Gagnon, D M
- Jabs, E W
- Wilkie, A O
Producer: 19970326
In:
Human molecular genetics vol. 6
Availability: No items available.
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10.
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A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. [electronic resource] by
- Muenke, M
- Gripp, K W
- McDonald-McGinn, D M
- Gaudenz, K
- Whitaker, L A
- Bartlett, S P
- Markowitz, R I
- Robin, N H
- Nwokoro, N
- Mulvihill, J J
- Losken, H W
- Mulliken, J B
- Guttmacher, A E
- Wilroy, R S
- Clarke, L A
- Hollway, G
- Adès, L C
- Haan, E A
- Mulley, J C
- Cohen, M M
- Bellus, G A
- Francomano, C A
- Moloney, D M
- Wall, S A
- Wilkie, A O
Producer: 19970318
In:
American journal of human genetics vol. 60
Availability: No items available.
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