You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


Advertisement

ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


Genetic Disorders

Citations 111-120 of 188 total displayed.

Past content (since May 1998):

Clinicopathologic Reports, Case Reports, and Small Case Series
Presenile Cataract: Consider Cholestanol
Alexandra Tészás; Zoltán Pfund; Éva Morava; György Kosztolányi; Erik Sistermans; Ron A. Wevers; Richard Kellermayer
Arch Ophthalmol 2006; 124: 1490-1492. [Extract] [Full text] [PDF]  

Clinicopathologic Reports, Case Reports, and Small Case Series
Familial Retinal Arterial Tortuosity Associated With Tortuosity in Nail Bed Capillaries
Florian Gekeler; Kei Shinoda; Michael Jünger; Karl Ulrich Bartz-Schmidt; Faik Gelisken
Arch Ophthalmol 2006; 124: 1492-1494. [Extract] [Full text] [PDF]  

Clinicopathologic Reports, Case Reports, and Small Case Series
Ligneous Conjunctivitis in a Mexican Patient With a Mutation in the Plasminogen (PLG) Gene
Juan M. Leyva-Castillo; Humberto Cavazos-Adame; Augusto Rojas-Martínez; Roberto López-Garza; Martin Cesar Fernandez Espinoza; Rocío Ortiz-López
Arch Ophthalmol 2006; 124: 1500-1501. [Extract] [Full text] [PDF]  

Ophthalmic Molecular Genetics
The Role of the WDR36 Gene on Chromosome 5q22.1 in a Large Family With Primary Open-Angle Glaucoma Mapped to This Region
Patricia L. Kramer; John R. Samples; Sharareh Monemi; Renee Sykes; Mansoor Sarfarazi; Mary K. Wirtz
Arch Ophthalmol 2006; 124: 1328-1331. [Abstract] [Full text] [PDF]  

Ophthalmic Molecular Genetics
Retinal Vein Occlusion Associated With Antithrombin Deficiency Secondary to a Novel G9840C Missense Mutation
Claudia Kuhli; Kristin Jochmans; Inge Scharrer; Marc Lüchtenberg; Lars-Olof Hattenbach
Arch Ophthalmol 2006; 124: 1165-1169. [Abstract] [Full text] [PDF]  

Editorials
How Much Influence Do Socioeconomic Factors Have on Glaucoma Prevalence and Therapeutic Outcomes?
Eve J. Higginbotham
Arch Ophthalmol 2006; 124: 1185-1186. [Extract] [Full text] [PDF]  

Ophthalmic Molecular Genetics
Clinical Findings in a Multigeneration Family With Autosomal Dominant Central Areolar Choroidal Dystrophy Associated With an Arg195Leu Mutation in the Peripherin/RDS Gene
Claudia N. Keilhauer; Thomas Meigen; Bernhard H. F. Weber
Arch Ophthalmol 2006; 124: 1020-1027. [Abstract] [Full text] [PDF]  

Editorials
Chase the Family
Harry A. Quigley
Arch Ophthalmol 2006; 124: 1036-1037. [Extract] [Full text] [PDF]  

Clinicopathologic Reports, Case Reports, and Small Case Series
Bilateral Macular Detachments in X-linked Retinoschisis
Sunir J. Garg; Henry C. Lee; M. Gilbert Grand
Arch Ophthalmol 2006; 124: 1053-1055. [Extract] [Full text] [PDF]  

Ophthalmic Molecular Genetics
Frequency of Retinal Cavernomas in 60 Patients With Familial Cerebral Cavernomas: A Clinical and Genetic Study
Pierre Labauge; Valerie Krivosic; Christian Denier; Elisabeth Tournier-Lasserve; Alain Gaudric
Arch Ophthalmol 2006; 124: 885-886. [Abstract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page]
Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19

 Collections
 •Sign up for Topic Collection Alerts
 •Topic Collections Home
 • Show Genetic Disorders
 collections from JAMA & Archives Journals.
 •Related collections:
  •Genetics
  •Genetic Counseling/ Testing/ Therapy
  •Genetic Disorders
  •Genetics, Other
Advertisement





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2009 American Medical Association. All Rights Reserved.