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Items: 1 to 20 of 92

1.

The Opitz trigonocephaly syndrome. A case report.

Oberklaid F, Danks DM.

Am J Dis Child. 1975 Nov;129(11):1348-9.

PMID:
1190170
2.

Opitz trigonocephaly syndrome.

Haaf T, Hofmann R, Schmid M.

Am J Med Genet. 1991 Sep 15;40(4):444-6.

PMID:
1746609
3.

A case of Kabuki (Niikawa-Kuroki) syndrome associated with manifestations resembling C-trigonocephaly syndrome.

David G, Sillence D, Hardwick R, Opitz JM.

Am J Med Genet A. 2004 Nov 1;130A(4):389-92.

PMID:
15389716
4.

Opitz "C" trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q.

Czakó M, Riegel M, Morava E, Bajnóczky K, Kosztolányi G.

Am J Med Genet A. 2004 Dec 15;131(3):310-2.

PMID:
15540175
5.

A new observation of acro-cardio-facial syndrome substantiates interindividual clinical variability.

Mingarelli R, Zuccarello D, Digilio MC, Dallapiccola B.

Am J Med Genet A. 2005 Jul 1;136(1):84-6. Review.

PMID:
15937946
6.

Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?

Bohring A, Silengo M, Lerone M, Superneau DW, Spaich C, Braddock SR, Poss A, Opitz JM.

Am J Med Genet. 1999 Aug 27;85(5):438-46. Review.

PMID:
10405439
7.

Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins.

Cleper R, Kauschansky A, Varsano I, Frydman M.

Am J Med Genet. 1993 Sep 15;47(4):451-5.

PMID:
8256802
8.

The G syndrome/Opitz oculo-genital-laryngeal syndrome/Opitz BBB/G syndrome/Opitz-Frias syndrome.

Conlon BJ, O'Dwyer T.

J Laryngol Otol. 1995 Mar;109(3):244-6.

PMID:
7745346
10.

[A typical case of Smith-Lemli-Opitz syndrome: nosologic problems and overlapping syndromes].

Camera G.

Pathologica. 1990 Sep-Oct;82(1081):539-42. Italian.

PMID:
1964208
11.

Congenital velopharyngeal incompetence in Kabuki make-up syndrome.

Lan K, Michiwaki Y, Sunaga S, Michi K.

Int J Oral Maxillofac Surg. 1995 Aug;24(4):298-300.

PMID:
7490494
12.

[Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome].

Franceschini P, Franceschini D.

Minerva Pediatr. 1994 Dec;46(12):579-80. Italian. No abstract available.

PMID:
7731422
13.

Velo-cardio-facial syndrome presenting as holoprosencephaly.

Wraith JE, Super M, Watson GH, Phillips M.

Clin Genet. 1985 Apr;27(4):408-10.

PMID:
3995791
14.

[Opitz' trigonocephaly syndrome].

Prager B, Hinkel GK, Lorenz P.

Kinderarztl Prax. 1991 Nov;59(11):346-8. German.

PMID:
1758140
15.

Smith-Lemli-Opitz syndrome. Case report.

Ruvalcaba RH, Reichert A, Smith DW.

Arch Dis Child. 1968 Oct;43(231):620-3. No abstract available.

16.

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
17.

Case report: femoral hypoplasia - unusual facies syndrome.

Pitt DB, Findlay II, Cole WG, Rogers JG.

Aust Paediatr J. 1982 Mar;18(1):63-6. No abstract available.

PMID:
7103883
18.

Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome.

Lubinsky M, Severn C, Rapoport JM.

Am J Med Genet. 1983 Mar;14(3):461-6.

PMID:
6859098
19.

[Velo-cardio-facial syndrome].

Kawame H.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):788-91. Review. Japanese. No abstract available.

PMID:
11529024
20.

Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.

Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B.

Ann Genet. 1992;35(4):208-12.

PMID:
1296516

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