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Craniosynostosis and kidney malformation in a case of Hennekam syndrome.
Cormier-Daire V, Lyonnet S, Lehnert A, Martin D, Salomon R, Patey N, Broyer M, Ricour C, Munnich A. Cormier-Daire V, et al. Among authors: salomon r. Am J Med Genet. 1995 May 22;57(1):66-8. doi: 10.1002/ajmg.1320570115. Am J Med Genet. 1995. PMID: 7645602
[Genetics of Hirschsprung disease].
Attié T, Amiel J, Jan D, Edery P, Pelet A, Salomon R, Munnich A, Lyonnet S, Nihoul-Fékété C. Attié T, et al. Among authors: salomon r. Ann Chir. 1996;50(7):538-41. Ann Chir. 1996. PMID: 9035423 French.
[Genetics of Hirschsprung disease].
Attié T, Salomon R, Amiel J, Edery P, Pelet A, Nihoul-Fékété C, Munnich A, Lyonnet S. Attié T, et al. Among authors: salomon r. C R Seances Soc Biol Fil. 1996;190(5-6):549-56. C R Seances Soc Biol Fil. 1996. PMID: 9074720 Review. French.
Mutations of the RET-GDNF signaling pathway in Ondine's curse.
Amiel J, Salomon R, Attié T, Pelet A, Trang H, Mokhtari M, Gaultier C, Munnich A, Lyonnet S. Amiel J, et al. Among authors: salomon r. Am J Hum Genet. 1998 Mar;62(3):715-7. doi: 10.1086/301759. Am J Hum Genet. 1998. PMID: 9497256 Free PMC article. No abstract available.
691 results