Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 88

1.

Familial pseudomarfanism, a new syndrome?

Dinno ND, Shearer L, Weisskopf B.

Birth Defects Orig Artic Ser. 1979;15(5B):179-88. No abstract available.

PMID:
316715
2.

The eye in the Marfan syndrome.

Maumenee IH.

Birth Defects Orig Artic Ser. 1982;18(6):515-24. No abstract available.

PMID:
6983370
3.

Familial simple ectopia lentis. A probable autosomal recessive form.

Ruiz C, Rivas F, Villar-Calvo VM, Serrano-Lucas JI, CantĂș JM.

Ophthalmic Paediatr Genet. 1986 Aug;7(2):81-4.

PMID:
3491351
4.

Isolated congenital ectopia lentis with autosomal dominant inheritance.

Jaureguy BM, Hall JG.

Clin Genet. 1979 Jan;15(1):97-109.

PMID:
310371
5.

Autosomal recessive ectopia lentis in two Arab family pedigrees.

al-Salem M.

Ophthalmic Paediatr Genet. 1990 Jun;11(2):123-7.

PMID:
2377351
6.

[Associated ectopia of the lens and pupil (apropos of 2 familial cases)].

Grange JD, Votan-Bonamour B.

Bull Soc Ophtalmol Fr. 1984 Jun-Jul;84(6-7):865-7. French. No abstract available.

PMID:
6335984
7.

[Congenital lens ectopia: apropos of 5 familial cases].

Saracco JB, Mouly A, Estachy G, Mortier JJ, Verdet R, Schillaci G.

Bull Soc Ophtalmol Fr. 1979 Feb;79(2):169-72. French. No abstract available.

PMID:
317436
8.

[Hereditary diseases with lens dislocation: clinical aspects].

Koepp P.

Klin Monbl Augenheilkd. 1987 Jan;190(1):8-10. German.

PMID:
3494881
9.

[Weill-Marchesani syndrome].

Herrera J, Morales M.

Rev Chil Pediatr. 1986 Nov-Dec;57(6):571-2. Spanish. No abstract available.

PMID:
3499643
10.

Ectopia lentis in a family.

Sinha A, Rahman A.

Indian J Ophthalmol. 1980 Apr;28(1):33-5. No abstract available.

11.

Clinical variability in the Marfan syndrome(s).

Pyeritz RE, Murphy EA, McKusick VA.

Birth Defects Orig Artic Ser. 1979;15(5B):155-78. No abstract available.

PMID:
526577
12.

Ectopia lentis.

Nelson LB, Maumenee IH.

Surv Ophthalmol. 1982 Nov-Dec;27(3):143-60.

PMID:
6984233
13.

Weill-Marchesani syndrome in mother and son.

Young ID, Fielder AR, Casey TA.

Clin Genet. 1986 Dec;30(6):475-80.

PMID:
3493095
14.

Familial simple ectopia lentis: a case study.

Casper DS, Simon JW, Nelson LB, Porter IH, Lichtenstein SB.

J Pediatr Ophthalmol Strabismus. 1985 Nov-Dec;22(6):227-30.

PMID:
3878400
15.

Ectopia lentis et pupillae.

Cross HE.

Am J Ophthalmol. 1979 Sep;88(3 Pt 1):381-4.

PMID:
314755
16.
17.

Dominantly inherited blepharoptosis, high myopia, and ectopia lentis.

Gillum WN, Anderson RL.

Arch Ophthalmol. 1982 Feb;100(2):282-4.

PMID:
6978128
18.

Hereditary ectopia lentis. A series of 10 cases of ectopia lentis et pupillae.

Meire FM.

Bull Soc Belge Ophtalmol. 1991;241:25-36.

PMID:
1840993
20.

Recessive mutations in LEPREL1 underlie a recognizable lens subluxation phenotype.

Khan AO, Aldahmesh MA, Alsharif H, Alkuraya FS.

Ophthalmic Genet. 2015 Mar;36(1):58-63. doi: 10.3109/13816810.2014.985847. Epub 2014 Dec 3.

PMID:
25469533

Supplemental Content

Support Center