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Genetic Disorders

Contributing journals to this collection:
JAMA & Archives Journals

Citations 61-70 of 1368 total displayed.

Past content

JAMA
The World in Medicine
Huntington Disease Setback
Joan Stephenson
JAMA 2009; 302: 732-b. [Extract] [Full text] [PDF]  

Arch Intern Med
Original Investigations
APOE Genotype, Lipids, and Coronary Heart Disease Risk: A Prospective Population Study
Heather Ward; Panagiota N. Mitrou; Richard Bowman; Robert Luben; Nicholas J. Wareham; Kay-Tee Khaw; Sheila Bingham
Arch Intern Med 2009; 169: 1424-1429. [Abstract] [Full text] [PDF]  

JAMA
Corrections
Incorrect Wording in: Interaction Between the Serotonin Transporter Gene (5-HTTLPR), Stressful Life Events, and Risk of Depression: A Meta-analysis
JAMA 2009; 302: 492. [Full text] [PDF]  

Arch Gen Psychiatry
Original Articles
Support for NRG1 as a Susceptibility Factor for Schizophrenia in a Northern Swedish Isolated Population
Maaike Alaerts; Shana Ceulemans; Diego Forero; Lotte N. Moens; Sonia De Zutter; Lien Heyrman; An-Sofie Lenaerts; Karl-Fredrik Norrback; Peter De Rijk; Lars-Göran Nilsson; Dirk Goossens; Rolf Adolfsson; Jurgen Del-Favero
Arch Gen Psychiatry 2009; 66: 828-837. [Abstract] [Full text] [PDF] [ eTables ]  

Arch Gen Psychiatry
Original Articles
Major Depression and Coronary Artery Disease in the Swedish Twin Registry: Phenotypic, Genetic, and Environmental Sources of Comorbidity
Kenneth S. Kendler; Charles O. Gardner; Amy Fiske; Margaret Gatz
Arch Gen Psychiatry 2009; 66: 857-863. [Abstract] [Full text] [PDF]  

Arch Neurol
Neurological Reviews
Progress and Challenges in RNA Interference Therapy for Huntington Disease
Scott Q. Harper
Arch Neurol 2009; 66: 933-938. [Abstract] [Full text] [PDF]  

Arch Neurol
Observations
Mitochondrial Neurogastrointestinal Encephalopathy Due to Mutations in RRM2B
Aziz Shaibani; Oleg A. Shchelochkov; Shulin Zhang; Panagiotis Katsonis; Olivier Lichtarge; Lee-Jun Wong; Marwan Shinawi
Arch Neurol 2009; 66: 1028-1032. [Abstract] [Full text] [PDF]  

Arch Ophthalmol
Research Letters
Novel Compound Heterozygous Mutations in CERKL Cause Autosomal Recessive Retinitis Pigmentosa in a Nonconsanguineous Chinese Family
Zhaohui Tang; Zhaoxiang Wang; Zhi Wang; Tie Ke; Qing Kenneth Wang; Mugen Liu
Arch Ophthalmol 2009; 127: 1077-1078. [Extract] [Full text] [PDF]  

JAMA
Medical News & Perspectives
FDA Focuses on Drugs and Liver Damage: Labeling and Other Changes for Acetaminophen
Bridget M. Kuehn
JAMA 2009; 302: 369-371. [Extract] [Full text] [PDF]  

JAMA
Health Agencies Update
New Inflammatory Disorder
Bridget M. Kuehn
JAMA 2009; 302: 375-c. [Extract] [Full text] [PDF]  

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