Author:
Bamshad Michael,Lin Robert C.,Law David J.,Watkins W. Scott,Krakowiak Patrycja A.,Moore Mary E.,Franceschini Piergiorgio,Lala Roberto,Holmes Lewis B.,Gebuhr Tom C.,Bruneau Benoit G.,Schinzel Albert,Seidman J. G.,Seidman Christine E.,Jorde Lynn B.
Publisher
Springer Science and Business Media LLC
Reference39 articles.
1. Leck, I. in Human Malformations and Related Anomalies. Vol.1 (eds. Stevenson, R.E., Hall, J.G. & Goodman, M.M.) 65–94 (Oxford University Press, Oxford, 1993).
2. Muragaki, Y., Mundlos, S., Upton, J. & Olson, B.R. Altered growth and branching patterns in synpolydactyly caused by mutations in HoxD13. Science. 272, 548–551 (1996).
3. Thomas, J.T. et al. A human chondrodysplasia due to a mutation in a TGF-beta superfamily member. Nature Genet. 12, 315–317 (1996).
4. Pallister, P.D., Herrmann, J. & Opitz, J.M. A pleiotropic dominant mutation affecting skeletal, sexual and apocrine-mammary development. Birth Defects Orig. Art. Ser. 12, 247–254 (1976).
5. Gonzales, C.H., Herrmann, J. & Opitz, J.M. Mother and son affected with the ulnar-mammary syndrome type Pallister. Eur. J. Pediatr. 123, 225–235 (1976).
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