CRANIOFACIAL SYNDROMES - NO SUCH THING AS A SINGLE-GENE DISEASE

[1] Aase JM, 1990, DIAGNOSTIC DYSMORPHO

[2] [Anonymous], 1994, MENDELIAN INHERITANC

[3] Cohen, 1986, CRANIOSYNOSTOSIS DIA

[4] SKELETAL ABNORMALITIES IN THE APERT SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (05): : 624 - 632

[5] A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES [J]. NATURE, 1994, 371 (6493) : 130 - 136

[6] EASTON DF, 1993, AM J HUM GENET, V53, P305

[7] FRANCOMANO CA, 1995, ONLINEMENDELIAN INHE

[8] Goodman R.M., 1983, MALFORMED INFANT CHI

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

[10] CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES - AUTOSOMAL DOMINANT PHENOTYPE IN A LARGE AMISH KINDRED [J]. JOURNAL OF PEDIATRICS, 1976, 88 (06) : 963 - 968

[1] Aase JM, 1990, DIAGNOSTIC DYSMORPHO

[2] [Anonymous], 1994, MENDELIAN INHERITANC

[3] Cohen, 1986, CRANIOSYNOSTOSIS DIA

[4] SKELETAL ABNORMALITIES IN THE APERT SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (05): : 624 - 632

[5] A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES [J]. NATURE, 1994, 371 (6493) : 130 - 136

[6] EASTON DF, 1993, AM J HUM GENET, V53, P305

[7] FRANCOMANO CA, 1995, ONLINEMENDELIAN INHE

[8] Goodman R.M., 1983, MALFORMED INFANT CHI

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

[10] CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES - AUTOSOMAL DOMINANT PHENOTYPE IN A LARGE AMISH KINDRED [J]. JOURNAL OF PEDIATRICS, 1976, 88 (06) : 963 - 968