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Items: 15

1.

Clinical ocular abnormalities in infants with trisomy 13.

Lueder GT.

Am J Ophthalmol. 2006 Jun;141(6):1057-60.

PMID:
16765673
2.

Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.

Monaghan KG, Van Dyke DL, Wiktor A, Feldman GL.

Am J Med Genet. 1997 Dec 12;73(2):180-3. Review.

PMID:
9409869
3.

CHARGE association: histopathological report of two cases and a review.

Hayashi N, Valdes-Dapena M, Green WR.

J Pediatr Ophthalmol Strabismus. 1998 Mar-Apr;35(2):100-6. Review.

PMID:
9559509
4.

Ocular manifestations of mosaic trisomy 22: a case report and review of the literature.

Thomas S, Parker M, Tan J, Duckett D, Woodruff G.

Ophthalmic Genet. 2004 Mar;25(1):53-6. Review.

PMID:
15255116
5.

[Ocular signs of trisomy 13. General review].

Cordier J, Reny A, Kahn N.

Adv Ophthalmol. 1971;24(0):174-202. Review. French. No abstract available.

PMID:
5006098
6.

An unusual patient with Rothmund-Thomson syndrome, porokeratosis and bilateral iris dysgenesis.

Mak RK, Griffiths WA, Mellerio JE.

Clin Exp Dermatol. 2006 May;31(3):401-3. Review.

PMID:
16681588
7.

Patau syndrome with a long survival (146 months): a clinical report and review of literature.

Iliopoulos D, Sekerli E, Vassiliou G, Sidiropoulou V, Topalidis A, Dimopoulou D, Voyiatzis N.

Am J Med Genet A. 2006 Jan 1;140(1):92-3. Review. No abstract available.

PMID:
16333832
8.
9.

Advances in the management of congenital and infantile cataract.

Lloyd IC, Ashworth J, Biswas S, Abadi RV.

Eye (Lond). 2007 Oct;21(10):1301-9. Review.

PMID:
17914433
10.

Ocular colobomata.

Onwochei BC, Simon JW, Bateman JB, Couture KC, Mir E.

Surv Ophthalmol. 2000 Nov-Dec;45(3):175-94. Review.

PMID:
11094243
11.

Congenital and developmental cataracts and multimalformation syndromes.

Bardelli AM, Lasorella G, Vanni M.

Ophthalmic Paediatr Genet. 1989 Dec;10(4):293-8. Review.

PMID:
2697825
12.

[Pseudo-trisomy 13 syndrome].

Kubota T.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):544. Review. Japanese. No abstract available.

PMID:
11528884
13.

[Rieger syndrome].

Makita Y.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):585-6. Review. Japanese. No abstract available.

PMID:
11528909
14.

[Cataracts-oto-dental defects (Nance-Horan syndrome)].

Sonoda T.

Ryoikibetsu Shokogun Shirizu. 2001;(33):344-5. Review. Japanese. No abstract available.

PMID:
11462467
15.

Trisomy 17-18. The clinical scope of a chromosomal aberration.

Taubert HD, Moszkowski EF, Saunders OH.

Md State Med J. 1966 Jun;15(6):48-55. Review. No abstract available.

PMID:
5327487
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