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Genetic Counseling/ Testing/ Therapy
Contributing journals to this collection:
JAMA & Archives Journals
Citations 461-470 of 718 total displayed.
- Correspondence
Identification of Novel Deletion Loci at 1p36 and 9p22-21 in Melanocytic Dysplastic Nevi and Cutaneous Malignant Melanomas
- Mahmoud R. Hussein; Eduardo Roggero; Ralph J. Tuthill; Gary S. Wood; Oscar Sudilovsky
Arch Dermatol 2003; 139: 816-817.
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- Original Contributions
Disease Course of Charcot-Marie-Tooth Disease Type 2: A 5-Year Follow-up Study
- Laurien L. Teunissen; Nicolette C. Notermans; Hessel Franssen; Baziel G. M. van Engelen; Frank Baas; John H. J. Wokke
Arch Neurol 2003; 60: 823-828.
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- Original Contributions
Frequency Analysis and Clinical Characterization of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 in Korean Patients
- Won Yong Lee; Dong Kyu Jin; Myung Ryurl Oh; Ji Eun Lee; Seng Mi Song; Eun Ah Lee; Gyeong-moon Kim; Jin Sang Chung; Kwang Ho Lee
Arch Neurol 2003; 60: 858-863.
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- Correspondence
Foveal Hypoplasia and Other Ocular Signs: A Possible Case of Incontinentia Pigmenti?
- Simon D. Chen; Richard Hanson; Kulwinder Hundal
Arch Ophthalmol 2003; 121: 921.
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- Medical News & Perspectives
Cause of Progeria's Premature Aging Found: Expected to Provide Insight Into Normal Aging Process
- Brian Vastag
JAMA 2003; 289: 2481-2482.
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- Basic Science Seminars in Neurology
Application of Microarrays to Neurological Disease
- Lisa-Marie Sturla; Ana Fernandez-Teijeiro; Scott L. Pomeroy
Arch Neurol 2003; 60: 676-682.
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- Original Contributions
A Common NURR1 Polymorphism Associated With Parkinson Disease and Diffuse Lewy Body Disease
- Kangni Zheng; Bobak Heydari; David K. Simon
Arch Neurol 2003; 60: 722-725.
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- Original Contributions
Molecular Diagnosis and Prophylactic Therapy for Presymptomatic Chinese Patients With Wilson Disease
- Zhi-Ying Wu; Min-Ting Lin; Shen-Xing Murong; Ning Wang
Arch Neurol 2003; 60: 737-741.
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- Papers
Multiple Endocrine Neoplasia Type 2: Evaluation of the Genotype-Phenotype Relationship
- Linwah Yip; Gilbert J. Cote; Suzanne E. Shapiro; Gregory D. Ayers; Cynthia E. Herzog; Rena V. Sellin; Steven I. Sherman; Robert F. Gagel; Jeffrey E. Lee; Douglas B. Evans
Arch Surg 2003; 138: 409-416.
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- Special Articles
Screening for Mutations in the MECP2 (Rett Syndrome) Gene in Gilles de la Tourette Syndrome
- Alberto L. Rosa; Joseph Jankovic; Tetsuo Ashizawa
Arch Neurol 2003; 60: 502-503.
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