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Items: 1 to 20 of 107

1.

Eating disorder in a patient with phenotypical features of Lujan-Fryns syndrome.

Alonso P, Pintos G, Almazan F, Hernández L, Loran E, Menchon JM, Vallejo J.

Clin Dysmorphol. 2006 Jul;15(3):181-4.

PMID:
16760741
2.

Preserved neurobehavioral abilities in Lujan-Fryns syndrome.

Donders J, Toriello H, van Doornik S.

Am J Med Genet. 2002 Jan 22;107(3):243-6.

PMID:
11807907
3.

Psychopathology in the Lujan-Fryns syndrome: report of two patients and review.

Lerma-Carrillo I, Molina JD, Cuevas-Duran T, Julve-Correcher C, Espejo-Saavedra JM, Andrade-Rosa C, Lopez-Muñoz F.

Am J Med Genet A. 2006 Dec 15;140(24):2807-11. Review.

PMID:
17036352
4.

Aortic root dilation in apparent Lujan-Fryns syndrome.

Wittine LM, Josephson KD, Williams MS.

Am J Med Genet. 1999 Oct 29;86(5):405-9.

PMID:
10508979
5.

Lujan-Fryns syndrome in the differential diagnosis of schizophrenia.

De Hert M, Steemans D, Theys P, Fryns JP, Peuskens J.

Am J Med Genet. 1996 Apr 9;67(2):212-4.

PMID:
8723050
6.

Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.

Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J.

Genet Couns. 1993;4(3):193-8.

PMID:
8267926
7.

Severe feeding difficulties in 3C syndrome.

Iyer P, Smith R.

Clin Dysmorphol. 2005 Apr;14(2):101-3.

PMID:
15770134
9.

Marfanoid features and X-linked mental retardation associated with craniofacial abnormalities: the Lujan-Fryns syndrome.

Dieckmann PM, Lucena LC, Dutra LA, Pedroso JL, Barsottini OG.

Arq Neuropsiquiatr. 2013 Jan;71(1):68-9. No abstract available.

10.

Tentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities?

Hackmann K, Rump A, Haas SA, Lemke JR, Fryns JP, Tzschach A, Wieczorek D, Albrecht B, Kuechler A, Ripperger T, Kobelt A, Oexle K, Tinschert S, Schrock E, Kalscheuer VM, Di Donato N.

Am J Med Genet A. 2016 Jan;170A(1):94-102. doi: 10.1002/ajmg.a.37378.

PMID:
26358559
11.

Newborn with anophthalmia and features of Fryns syndrome.

Pierson DM, Subtil A, Taboada E, Butler MG.

Pediatr Dev Pathol. 2002 Nov-Dec;5(6):592-6.

PMID:
12375132
12.

Neuropsychological evaluation in Lujan-Fryns syndrome: commentary and clinical report.

Williams MS.

Am J Med Genet A. 2006 Dec 15;140(24):2812-5. No abstract available.

PMID:
17103446
13.

Café au lait macules and cerebro-oculo-facio-skeletal syndrome: a novel association.

Twede JV, Difazio M.

Pediatr Dermatol. 2009 Jan-Feb;26(1):97-9. doi: 10.1111/j.1525-1470.2008.00833.x.

PMID:
19250421
14.

Eye abnormalities in Fryns syndrome.

Pierson DM, Taboada E, Butler MG.

Am J Med Genet A. 2004 Mar 15;125A(3):273-7.

PMID:
14994236
15.

[Fryns syndrome. Report on 3 new cases].

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

Arch Pediatr. 2007 Jul;14(7):903-7. French.

PMID:
17442547
16.

Food aversion and facial dysmorphism--a newly described syndrome?

Keng WT, Cole T, Pilz D, Porteous ME.

Clin Dysmorphol. 2002 Oct;11(4):249-53.

PMID:
12401989
17.

A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions.

Baynam G, Goldblatt J, Townshend S.

Clin Dysmorphol. 2006 Jul;15(3):145-8. Review.

PMID:
16760732
18.

Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus).

Van Buggenhout G, Fryns JP.

Orphanet J Rare Dis. 2006 Jul 10;1:26. Review.

19.

Characterizing the oculoauriculofrontonasal syndrome.

Gabbett MT, Robertson SP, Broadbent R, Aftimos S, Sachdev R, Nezarati MM.

Clin Dysmorphol. 2008 Apr;17(2):79-85. doi: 10.1097/MCD.0b013e3282f449c8.

PMID:
18388775
20.

Etiology of chest wall deformities--a genetic review for the treating physician.

Kotzot D, Schwabegger AH.

J Pediatr Surg. 2009 Oct;44(10):2004-11. doi: 10.1016/j.jpedsurg.2009.07.029. Review.

PMID:
19853763
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