Genetic Disorders

Contributing journals to this collection:
JAMA & Archives Journals

Citations 461-470 of 1368 total displayed.

Past content

The World in Medicine
Pseudomonas Vaccine

Joan Stephenson
JAMA 2007; 298: 277-c. [Extract] [Full text] [PDF]  

Medical News & Perspectives
Researchers Report New Clues to Dementia

M. J. Friedrich
JAMA 2007; 298: 161-163. [Extract] [Full text] [PDF]  

Original Articles
An Epigenetically Derived Monoclonal Origin for Recurrent Respiratory Papillomatosis

Josena Kunjoonju Stephen; Lori E. Vaught; Kang Mei Chen; Veena Shah; Vanessa G. Schweitzer; Glendon Gardner; Michael S. Benninger; Maria J. Worsham
Arch Otolaryngol Head Neck Surg 2007; 133: 684-692. [Abstract] [Full text] [PDF]  

Original Articles
Cortical Brain Development in Nonpsychotic Siblings of Patients With Childhood-Onset Schizophrenia

Nitin Gogtay; Deanna Greenstein; Marge Lenane; Liv Clasen; Wendy Sharp; Pete Gochman; Philip Butler; Alan Evans; Judith Rapoport
Arch Gen Psychiatry 2007; 64: 772-780. [Abstract] [Full text] [PDF]  

Original Articles
Intergenerational Transmission of Childhood Conduct Problems: A Children of Twins Study

Brian M. D’Onofrio; Wendy S. Slutske; Eric Turkheimer; Robert E. Emery; K. Paige Harden; Andrew C. Heath; Pamela A. F. Madden; Nicholas G. Martin
Arch Gen Psychiatry 2007; 64: 820-829. [Abstract] [Full text] [PDF]  

Ophthalmic Molecular Genetics
Novel Compound Heterozygous TULP1 Mutations in a Family With Severe Early-Onset Retinitis Pigmentosa

Anneke I. den Hollander; Janneke J. C. van Lith-Verhoeven; Maarten L. Arends; Tim M. Strom; Frans P. M. Cremers; Carel B. Hoyng
Arch Ophthalmol 2007; 125: 932-935. [Abstract] [Full text] [PDF]  

Editorials
Dwindling Indications for Sural Nerve Biopsy

David E. Pleasure
Arch Neurol 2007; 64: 935-936. [Extract] [Full text] [PDF]  

Neurological Reviews
The New Neurobiology of Autism: Cortex, Connectivity, and Neuronal Organization

Nancy J. Minshew; Diane L. Williams
Arch Neurol 2007; 64: 945-950. [Abstract] [Full text] [PDF]  

Original Contributions
Clinical and Electrophysiological Features in Charcot-Marie-Tooth Disease With Mutations in the NEFL Gene

Gabriel Miltenberger-Miltenyi; Andreas R. Janecke; Julia V. Wanschitz; Vincent Timmerman; Christian Windpassinger; Michaela Auer-Grumbach; Wolfgang N. Löscher
Arch Neurol 2007; 64: 966-970. [Abstract] [Full text] [PDF]  

Original Contributions
Stoichiometric Alteration of PMP22 Protein Determines the Phenotype of Hereditary Neuropathy With Liability to Pressure Palsies

Jun Li; Khaled Ghandour; Danijela Radovanovic; Rosemary R. Shy; Karen M. Krajewski; Michael E. Shy; Garth A. Nicholson
Arch Neurol 2007; 64: 974-978. [Abstract] [Full text] [PDF]  

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