Genetic Counseling/ Testing/ Therapy

Contributing journals to this collection:
JAMA & Archives Journals

Citations 441-450 of 718 total displayed.

Past content

The Pediatric Forum
Need for Genetic Education for Type 1 Diabetes—Reply

Lainie F. Ross
Arch Pediatr Adolesc Med 2003; 157: 936. [Extract] [Full text] [PDF]  

Studies
Clinical Study of 40 Cases of Incontinentia Pigmenti

Smaïl Hadj-Rabia; David Froidevaux; Nathalie Bodak; Dominique Hamel-Teillac; Asma Smahi; Yasmina Touil; Sylvie Fraitag; Yves de Prost; Christine Bodemer
Arch Dermatol 2003; 139: 1163-1170. [Abstract] [Full text] [PDF]  

Corrections
Frequency Analysis and Clinical Characterization of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 in Korean Patients—Correction

Arch Neurol 2003; 60: 1256. [Full text] [PDF]  

Original Contributions
Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase

Massimiliano Filosto; Michelangelo Mancuso; Yutaka Nishigaki; Jacklyn Pancrudo; Yadollah Harati; Clifton Gooch; Ami Mankodi; Lydia Bayne; Eduardo Bonilla; Sara Shanske; Michio Hirano; Salvatore DiMauro
Arch Neurol 2003; 60: 1279-1284. [Abstract] [Full text] [PDF]  

Original Articles
Altered Gene Expression of Brain-Derived Neurotrophic Factor and Receptor Tyrosine Kinase B in Postmortem Brain of Suicide Subjects

Yogesh Dwivedi; Hooriyah S. Rizavi; Robert R. Conley; Rosalinda C. Roberts; Carol A. Tamminga; Ghanshyam N. Pandey
Arch Gen Psychiatry 2003; 60: 804-815. [Abstract] [Full text] [PDF]  

Neurological Reviews
The Hereditary Spastic Paraplegias: Nine Genes and Counting

John K. Fink
Arch Neurol 2003; 60: 1045-1049. [Abstract] [Full text] [PDF]  

Clinical Sciences
Clinical Description and Exclusion of Candidate Genes in a Novel Autosomal Recessively Inherited Vitreoretinal Dystrophy

Gian-Marco Sarra; Maike Weigell-Weber; Dieter Kotzot; Günter Niemeyer; Elmar Messmer; Martin Hergersberg
Arch Ophthalmol 2003; 121: 1109-1116. [Abstract] [Full text] [PDF]  

Ophthalmic Molecular Genetics
Genomewide Homozygosity Mapping and Molecular Analysis of a Candidate Gene Located on 22q13 (Fibulin-1) in a Previously Undescribed Vitreoretinal Dystrophy

Maike Weigell-Weber; Gian-Marco Sarra; Dieter Kotzot; Lodewijk Sandkuijl; Elmar Messmer; Martin Hergersberg
Arch Ophthalmol 2003; 121: 1184-1188. [Abstract] [Full text] [PDF]  

Medical News & Perspectives
UK Licenses Human Embryo Creation: "Dolly" Cloner to Create Embryos for Research

Brian Vastag
JAMA 2003; 290: 449-450. [Extract] [Full text] [PDF]  

Original Articles
Delineating Genetic Pathways of Disease Progression in Head and Neck Squamous Cell Carcinoma

Maria J. Worsham; Gerard Pals; Jan P. Schouten; Rosalind M. L. van Spaendonk; Adriane Concus; Thomas E. Carey; Michael S. Benninger
Arch Otolaryngol Head Neck Surg 2003; 129: 702-708. [Abstract] [Full text] [PDF]  

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