Twist and shout

[11] HARTENSTEIN V, 1985, Wilhelm Roux's Archives of Developmental Biology, V194, P213, DOI 10.1007/BF00848248

[12] THE DIASTROPHIC DYSPLASIA GENE ENCODES A NOVEL SULFATE TRANSPORTER - POSITIONAL CLONING BY FINE-STRUCTURE LINKAGE DISEQUILIBRIUM MAPPING [J]. CELL, 1994, 78 (06) : 1073 - 1087

[13] Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 36 - 41

[14] A MOUSE MODEL OF GREIG CEPHALOPOLYSYNDACTYLY SYNDROME - THE EXTRA-TOES(J) MUTATION CONTAINS AN INTRAGENIC DELETION OF THE GLI3 GENE [J]. NATURE GENETICS, 1993, 3 (03) : 241 - 246

[15] JACKSON-WEISS-SYNDROME AND CROUZON-SYNDROME ARE ALLELIC WITH MUTATIONS IN FIBROBLAST GROWTH-FACTOR RECEPTOR-2 [J]. NATURE GENETICS, 1994, 8 (03) : 275 - 279

[16] A MUTATION IN THE HOMEODOMAIN OF THE HUMAN MSX2 GENE IN A FAMILY AFFECTED WITH AUTOSOMAL-DOMINANT CRANIOSYNOSTOSIS [J]. CELL, 1993, 75 (03) : 443 - 450

[17] Li QY, 1997, NAT GENET, V15, P21

[18] THE B-HLH PROTEIN ENCODING THE M-TWIST GENE IS LOCATED BY INSITU HYBRIDIZATION ON MURINE CHROMOSOME-12 [J]. MAMMALIAN GENOME, 1993, 4 (02) : 127 - 128

[19] A COMMON MUTATION IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-1 GENE IN PFEIFFER-SYNDROME [J]. NATURE GENETICS, 1994, 8 (03) : 269 - 274

[20] ASSIGNMENT OF A GENE LOCUS INVOLVED IN CRANIOSYNOSTOSIS TO CHROMOSOME-5QTER [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (02) : 119 - 122

[11] HARTENSTEIN V, 1985, Wilhelm Roux's Archives of Developmental Biology, V194, P213, DOI 10.1007/BF00848248

[12] THE DIASTROPHIC DYSPLASIA GENE ENCODES A NOVEL SULFATE TRANSPORTER - POSITIONAL CLONING BY FINE-STRUCTURE LINKAGE DISEQUILIBRIUM MAPPING [J]. CELL, 1994, 78 (06) : 1073 - 1087

[13] Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 36 - 41

[14] A MOUSE MODEL OF GREIG CEPHALOPOLYSYNDACTYLY SYNDROME - THE EXTRA-TOES(J) MUTATION CONTAINS AN INTRAGENIC DELETION OF THE GLI3 GENE [J]. NATURE GENETICS, 1993, 3 (03) : 241 - 246

[15] JACKSON-WEISS-SYNDROME AND CROUZON-SYNDROME ARE ALLELIC WITH MUTATIONS IN FIBROBLAST GROWTH-FACTOR RECEPTOR-2 [J]. NATURE GENETICS, 1994, 8 (03) : 275 - 279

[16] A MUTATION IN THE HOMEODOMAIN OF THE HUMAN MSX2 GENE IN A FAMILY AFFECTED WITH AUTOSOMAL-DOMINANT CRANIOSYNOSTOSIS [J]. CELL, 1993, 75 (03) : 443 - 450

[17] Li QY, 1997, NAT GENET, V15, P21

[18] THE B-HLH PROTEIN ENCODING THE M-TWIST GENE IS LOCATED BY INSITU HYBRIDIZATION ON MURINE CHROMOSOME-12 [J]. MAMMALIAN GENOME, 1993, 4 (02) : 127 - 128

[19] A COMMON MUTATION IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-1 GENE IN PFEIFFER-SYNDROME [J]. NATURE GENETICS, 1994, 8 (03) : 269 - 274

[20] ASSIGNMENT OF A GENE LOCUS INVOLVED IN CRANIOSYNOSTOSIS TO CHROMOSOME-5QTER [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (02) : 119 - 122