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Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. [electronic resource] by
- Howard, T D
- Paznekas, W A
- Green, E D
- Chiang, L C
- Ma, N
- Ortiz de Luna, R I
- Garcia Delgado, C
- Gonzalez-Ramos, M
- Kline, A D
- Jabs, E W
Producer: 19970128
In:
Nature genetics vol. 15
Availability: No items available.
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15.
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Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations. [electronic resource] by
- Paznekas, W A
- Cunningham, M L
- Howard, T D
- Korf, B R
- Lipson, M H
- Grix, A W
- Feingold, M
- Goldberg, R
- Borochowitz, Z
- Aleck, K
- Mulliken, J
- Yin, M
- Jabs, E W
Producer: 19980624
In:
American journal of human genetics vol. 62
Availability: No items available.
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16.
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Physical map of the chromosome 6q22 region containing the oculodentodigital dysplasia locus: analysis of thirteen candidate genes and identification of novel ESTs and DNA polymorphisms. [electronic resource] by
- Boyadjiev, S A
- Chowdry, A B
- Shapiro, R E
- Paznekas, W A
- Wandstrat, A E
- Choi, J W
- Kasch, L
- Zhang, G
- Wollnik, B
- Burgess, C E
- Schalling, M
- Lovett, M
- Jabs, E W
Producer: 20030404
In:
Cytogenetic and genome research vol. 98
Availability: No items available.
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