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Items: 1 to 20 of 81

1.

Gordon syndrome: literature review and a report of two cases.

Botha SJ, Bütow KW.

Cleft Palate Craniofac J. 2015 Jan;52(1):e18-22. doi: 10.1597/13-075.

PMID:
24878349
2.
3.

The Gordon syndrome: autosomal dominant cleft palate, camptodactyly, and club feet.

Robinow M, Johnson GF.

Am J Med Genet. 1981;9(2):139-46.

PMID:
7258227
4.

The distal arthrogryposes: delineation of new entities--review and nosologic discussion.

Hall JG, Reed SD, Greene G.

Am J Med Genet. 1982 Feb;11(2):185-239. Review.

PMID:
7039311
5.

Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia.

Stamm DS, Aylsworth AS, Stajich JM, Kahler SG, Thorne LB, Speer MC, Powell CM.

Am J Med Genet A. 2008 Jul 15;146A(14):1832-41. doi: 10.1002/ajmg.a.32370.

PMID:
18553514
6.
7.
8.

Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndrome.

Ioan DM, Belengeanu V, Maximilian C, Fryns JP.

Clin Genet. 1993 Jun;43(6):300-2.

PMID:
8370149
9.

A rare case of 3C disease: Ritscher-Schinzel syndrome presenting with recurrent talipes equinovarus.

Konya MN, Elmas M, Erginoğlu SE, Yeşil M.

Int J Surg Case Rep. 2015;7C:130-3. doi: 10.1016/j.ijscr.2014.10.098. Epub 2014 Nov 6.

10.

Congenital myopathy with cleft palate and increased susceptibility to malignant hyperthermia: King syndrome?

Stewart CR, Kahler SG, Gilchrist JM.

Pediatr Neurol. 1988 Nov-Dec;4(6):371-4.

PMID:
3245876
11.

Extending the spectrum of distal arthrogryposis.

Gripp KW, Scott CI Jr, Brockett BC, Nicholson L, Mackenzie WG.

Am J Med Genet. 1996 Nov 11;65(4):286-90.

PMID:
8923937
12.
13.

Diagnostic considerations in arthrogryposis syndromes in South Africa.

Gericke GS, Hall JG, Nelson MM, Beighton PH.

Clin Genet. 1984 Feb;25(2):155-62.

PMID:
6538466
14.
15.

Familial Gordon syndrome associated with a PIEZO2 mutation.

Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D.

Am J Med Genet A. 2017 Jan;173(1):254-259. doi: 10.1002/ajmg.a.37997. Epub 2016 Oct 7.

PMID:
27714920
16.

Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations.

Chadwick B, Hunter B, Hunter L, Aldred M, Wilkie A.

Oral Surg Oral Med Oral Pathol. 1994 Jul;78(1):57-63. Review.

PMID:
8078665
17.

New syndrome or severe expression of Gordon syndrome? A case report.

Courtens W, Perlmutter N, Dan B, Vamos E.

Clin Dysmorphol. 1997 Jan;6(1):39-44.

PMID:
9018417
18.

An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE).

Giannotti A, Digilio MC, Mingarelli R, Dallapiccola B.

J Med Genet. 1995 Jan;32(1):72-4.

19.

A case report of Gordon's syndrome in a 20-year-old male with free medical family history.

Kostakis ID, Tsoukalas NG, Aravantinos DC, Gkizis IG, Cholidou KG, Papadopoulos DP.

Hellenic J Cardiol. 2013 Jan-Feb;54(1):64-8.

20.

The Gordon syndrome revisited.

Basel D, Sobey G, Gardner J, Beighton P.

S Afr Med J. 2000 Sep;90(9):864-7. No abstract available.

PMID:
11081133

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