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Items: 4

1.

Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome.

Sood S, Eldadah ZA, Krause WL, McIntosh I, Dietz HC.

Nat Genet. 1996 Feb;12(2):209-11.

PMID:
8563763
2.

Response to Anesthetic management of a rare case of Shprintzen-Goldberg craniosynostosis syndrome.

Gupta A, Bathla S, Saini S, Kamal G.

Paediatr Anaesth. 2010 Dec;20(12):1138. doi: 10.1111/j.1460-9592.2010.03451.x. No abstract available.

PMID:
21199127
3.

Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull.

Saal HM, Bulas DI, Allen JF, Vezina LG, Walton D, Rosenbaum KN.

Am J Med Genet. 1995 Jul 17;57(4):573-8. Review.

PMID:
7573131
4.

Anesthetic management of a rare case of Shprintzen-Goldberg craniosynostosis syndrome.

Gupta AK, Divekar DS, Shah B, Dhulkhed VK.

Paediatr Anaesth. 2010 Aug;20(8):771-3. doi: 10.1111/j.1460-9592.2010.03340.x. No abstract available.

PMID:
20670243

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