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Items: 1 to 20 of 252

1.

"C" trigonocephaly syndrome with diaphragmnatic hernia.

Addor MC, Stefanutti D, Farron F, Meinecke P, Lacombe D, Sarlangue J, Prescia G, Schorderet DF.

Genet Couns. 1995;6(2):113-20.

PMID:
7546453
2.

Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly.

Schaap C, Schrander-Stumpel CT, Fryns JP.

Genet Couns. 1992;3(4):209-15. Review.

PMID:
1472356
3.

[Fryns syndrome: report of the first case in the national literature].

Rentería-Ibarra M, Frías-Márquez SG, Michel-Aceves RJ, Navarrete-Arellano M.

Bol Med Hosp Infant Mex. 1993 Sep;50(9):666-70. Spanish.

PMID:
8373549
4.

Fryns syndrome: another example of non-lethal outcome with severe mental handicap.

Hanssen AM, Schrander-Stumpel CT, Thiry PA, Fryns JP.

Genet Couns. 1992;3(4):187-93.

PMID:
1472353
5.

[Genetic morphological fatal syndromes. The Fryns syndrome].

Henkel KE, Pfeiffer RA, Stöss H.

Pathologe. 1993 Mar;14(2):92-3. German. No abstract available.

PMID:
8469652
6.
7.

"C" trigonocephaly syndrome: two additional cases.

Camera G, Serra G, Selicorni A.

Am J Med Genet. 1990 Dec;37(4):463-4. No abstract available.

PMID:
2260588
8.

Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.

Fryns JP, Vogels A, Haegeman J, Eggermont E, van den Berghe H.

Genet Couns. 1994;5(4):337-43.

PMID:
7888135
9.

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG.

Am J Med Genet. 1989 Jan;32(1):93-9.

PMID:
2650550
10.

[Opitz-trigonocephaly syndrome--a characteristic dysmorphia-retardation syndrome of unclear origin].

Choudhury AR, Renneberg A, Rackowitz A, Stephani U.

Klin Padiatr. 1992 May-Jun;204(3):171-3. Review. German.

PMID:
1614184
11.

"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.

Lalatta F, Clerici Bagozzi D, Salmoiraghi MG, Tagliabue P, Tischer C, Zollino M, Di Rocco C, Neri G, Opitz JM.

Am J Med Genet. 1990 Dec;37(4):451-6.

PMID:
2260586
12.

The Miller-Dieker syndrome: a case report and review of the literature.

Izmeth MG, Parameshwar E.

J Ment Defic Res. 1989 Jun;33 ( Pt 3):267-70. Review.

PMID:
2666671
13.

Fryns syndrome survivors and neurologic outcome.

Van Hove JL, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla AK, Kahler SG.

Am J Med Genet. 1995 Nov 20;59(3):334-40. Review.

PMID:
8599357
14.

Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.

Casaccia G, Mobili L, Braguglia A, Santoro F, Bagolan P.

Birth Defects Res A Clin Mol Teratol. 2006 Mar;76(3):210-3.

PMID:
16498629
15.

Trigonocephaly and the Opitz C syndrome.

Sargent C, Burn J, Baraitser M, Pembrey ME.

J Med Genet. 1985 Feb;22(1):39-45.

16.

Fryns syndrome: a lethal mesoectodermal birth defect with variable expression in a pair of monozygotic twins.

Pratap A, Agrawal A, Raja S, Khaniya S, Tiwari A, Kumar A.

Singapore Med J. 2007 Apr;48(4):e106-8.

17.

Craniofrontonasal dysplasia: more severe expression in the mother than in her son.

Devriendt K, Van Mol C, Fryns JP.

Genet Couns. 1995;6(4):361-4.

PMID:
8775424
18.

Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature.

Alessandri L, Brayer C, Attali T, Samperiz S, Tiran-Rajaofera I, Ramful D, Pilorget H.

Genet Couns. 2005;16(4):363-70. Review.

PMID:
16440878
19.

Costello syndrome: the natural history of a true postnatal growth retardation syndrome.

Umans S, Decock P, Fryns JP.

Genet Couns. 1995;6(2):121-5.

PMID:
7546454
20.

FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.

Zwamborn-Hanssen AM, Schrander-Stumpel CT, Smeets E, Decock P, Fryns JP.

Genet Couns. 1995;6(4):313-9.

PMID:
8775418

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