Related Articles by Review for PMID: 9182791

Year	Number of Results
1995	2
1997	1
1998	1
2000	1
2001	1
2002	1
2006	1
2013	1
2014	1
2016	1
2024	0

1

Shprintzen-Goldberg syndrome with osteopenia and progressive hydrocephalus.

Hassed S, Shewmake K, Teo C, Curtis M, Cunniff C. Hassed S, et al. Am J Med Genet. 1997 Jun 27;70(4):450-3. Am J Med Genet. 1997. PMID: 9182791 No abstract available.

2

Shprintzen-Goldberg syndrome: a clinical analysis.

Greally MT, Carey JC, Milewicz DM, Hudgins L, Goldberg RB, Shprintzen RJ, Cousineau AJ, Smith WL Jr, Judisch GF, Hanson JW. Greally MT, et al. Am J Med Genet. 1998 Mar 19;76(3):202-12. Am J Med Genet. 1998. PMID: 9508238 Review.

3

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome.

Adès LC, Morris LL, Power RG, Wilson M, Haan EA, Bateman JF, Milewicz DM, Sillence DO. Adès LC, et al. Am J Med Genet. 1995 Jul 17;57(4):565-72. doi: 10.1002/ajmg.1320570410. Am J Med Genet. 1995. PMID: 7573130 Review.

4

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

Saal HM, Bulas DI, Allen JF, Vezina LG, Walton D, Rosenbaum KN. Saal HM, et al. Am J Med Genet. 1995 Jul 17;57(4):573-8. doi: 10.1002/ajmg.1320570411. Am J Med Genet. 1995. PMID: 7573131 Review.

5

Dysplasia of C-1 and craniocervical instability in patients with Shprintzen-Goldberg syndrome. Case report and review of the literature.

Jödicke A, Hahn A, Berthold LD, Scharbrodt W, Böker DK. Jödicke A, et al. J Neurosurg. 2006 Sep;105(3 Suppl):238-41. doi: 10.3171/ped.2006.105.3.238. J Neurosurg. 2006. PMID: 16970241 Review.

6

De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: two new cases and a clinical review.

Au PY, Racher HE, Graham JM Jr, Kramer N, Lowry RB, Parboosingh JS, Innes AM; FORGE Canada Consortium. Au PY, et al. Am J Med Genet A. 2014 Mar;164A(3):676-84. doi: 10.1002/ajmg.a.36340. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357594 Review.

7

Shprintzen-Goldberg syndrome: a rare disorder.

Yadav S, Rawal G. Yadav S, et al. Pan Afr Med J. 2016 Apr 25;23:227. doi: 10.11604/pamj.2016.23.227.7482. eCollection 2016. Pan Afr Med J. 2016. PMID: 27761171 Free PMC article. Review.

8

Possible third case of Lin-Gettig syndrome.

Hedera P, Innis JW. Hedera P, et al. Am J Med Genet. 2002 Jul 15;110(4):380-3. doi: 10.1002/ajmg.10460. Am J Med Genet. 2002. PMID: 12116213 Free article. Review.

9

[Cloverleaf skull syndrome].

EnomotoT, Fujimoto A. EnomotoT, et al. Ryoikibetsu Shokogun Shirizu. 2000;(28 Pt 3):578-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11221642 Review. Japanese. No abstract available.

10

[Pharynx/larynx hypoplasia-omphalocele, Shprintzen-Goldberg type].

Ishida S, Fukushima Y. Ishida S, et al. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):500-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528862 Review. Japanese. No abstract available.

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