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Items: 1 to 20 of 160

1.

Schinzel-Giedion syndrome: report of two sibs.

Antich J, Manzanares R, Camarasa F, Krauel X, Vila J, Cusi V.

Am J Med Genet. 1995 Oct 23;59(1):96-9.

PMID:
8849020
2.

Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis.

Albano LM, Sakae PP, Mataloun MM, Leone CR, Bertola DR, Kim CA.

Rev Hosp Clin Fac Med Sao Paulo. 2004 Apr;59(2):89-92. Epub 2004 Apr 26.

3.

Schinzel-Giedion syndrome with sacrococcygeal teratoma.

Sandri A, Manazza AD, Bertin D, Silengo M, Basso ME, Forni M, Madon E.

J Pediatr Hematol Oncol. 2003 Jul;25(7):558-61.

PMID:
12847324
4.

Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype.

Ozkinay FF, Akisü M, Kültürsay N, Oral R, Tansug N, Sapmaz G.

Clin Genet. 1996 Sep;50(3):145-8.

PMID:
8946113
5.

Three new cases of the Schinzel-Giedion syndrome and review of the literature.

Labrune P, Lyonnet S, Zupan V, Imbert MC, Goutieres F, Hubert P, Le Merrer M.

Am J Med Genet. 1994 Mar 1;50(1):90-3. Review.

PMID:
8160760
7.

Schinzel-Giedion syndrome.

Verloes A, Moës D, Palumbo L, Elmer C, François A, Bricteux G.

Eur J Pediatr. 1993 May;152(5):421-3.

PMID:
8319710
8.

New finding of Schinzel-Giedion syndrome: a case with a malignant sacrococcygeal teratoma.

Robin NH, Grace K, DeSouza TG, McDonald-McGinn D, Zackai EH.

Am J Med Genet. 1993 Nov 1;47(6):852-6.

PMID:
7506484
9.

A patient with Schinzel-Giedion syndrome and a review of 20 patients.

Okamoto N, Takeuchi M, Kitajima H, Hosokawa S.

Jpn J Hum Genet. 1995 Jun;40(2):189-93. Review.

PMID:
7662999
10.

Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.

Rodríguez JI, Jiménez-Heffernan JA, Leal J.

Am J Med Genet. 1994 Dec 1;53(4):374-7.

PMID:
7864048
11.

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Lehman AM, McFadden D, Pugash D, Sangha K, Gibson WT, Patel MS.

Am J Med Genet A. 2008 May 15;146A(10):1299-306. doi: 10.1002/ajmg.a.32277.

PMID:
18398855
12.

A Schinzel-Giedion-like syndrome--a milder version or a separate condition?

Joss S, Dean JC.

Clin Dysmorphol. 2002 Oct;11(4):271-5.

PMID:
12401993
13.

Schinzel-Giedion syndrome: further delineation of the phenotype.

Elliott AM, Meagher-Villemure K, Oudjhane K, der Kaloustian VM.

Clin Dysmorphol. 1996 Apr;5(2):135-42. Review.

PMID:
8723563
14.

Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p.

Le Caignec C, Winer N, Boceno M, Delnatte C, Podevin G, Liet JM, Quere MP, Joubert M, Rival JM.

Prenat Diagn. 2003 Dec 15;23(12):981-4. Review.

PMID:
14663834
15.

The Schinzel-Giedion syndrome.

al-Gazali LI, Farndon P, Burn J, Flannery DB, Davison C, Mueller RF.

J Med Genet. 1990 Jan;27(1):42-7. Review. No abstract available.

16.

Sister and brother with Vici syndrome: agenesis of the corpus callosum, albinism, and recurrent infections.

Chiyonobu T, Yoshihara T, Fukushima Y, Yamamoto Y, Tsunamoto K, Nishimura Y, Ishida H, Toda T, Kasubuchi Y.

Am J Med Genet. 2002 Apr 15;109(1):61-6. Review.

PMID:
11932994
17.
18.

Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.

Santos H, Cordeiro I, Medeira A, Mendonça E, Antunes NL, Rosa FC.

Genet Couns. 1994;5(2):187-9.

PMID:
7917131
19.

New case of Toriello-Carey syndrome.

Lacombe D, Creusot G, Battin J.

Am J Med Genet. 1992 Feb 1;42(3):374-6.

PMID:
1536182
20.

Further delineation of the Toriello-Carey syndrome: a report of two siblings.

Barisic I, Peter B, Mikecin L.

Am J Med Genet A. 2003 Jan 15;116A(2):188-91.

PMID:
12494442

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