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Download e-book for iPad: Amyotrophic Lateral Sclerosis - A Bibliography and by Philip M. Parker

By Philip M. Parker

ISBN-10: 0497113279

ISBN-13: 9780497113278

ISBN-10: 142949610X

ISBN-13: 9781429496100

In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: ''The variety of sites supplying health-related assets grows each day. Many websites offer helpful info, whereas others could have details that's unreliable or misleading.'' in addition, a result of swift elevate in Internet-based details, many hours could be wasted looking out, settling on, and printing. on account that basically the smallest fraction of knowledge facing Amyotrophic lateral sclerosis is listed in se's, akin to or others, a non-systematic method of web study could be not just time eating, but in addition incomplete. This publication used to be created for doctors, scholars, and individuals of most people who are looking to behavior scientific examine utilizing the main complicated instruments on hand and spending the smallest amount of time doing so.

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Extra resources for Amyotrophic Lateral Sclerosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Review. S. Government supports a variety of research studies relating to amyotrophic lateral sclerosis. 11 CRISP (Computerized Retrieval of Information on Scientific Projects) CRISP is a searchable database of federally funded biomedical research projects conducted at universities, hospitals, and other institutions. generate_screen. You will have the option to perform targeted searches by various criteria, including geography, date, and topics related to amyotrophic lateral sclerosis. For most of the studies, the agencies reporting into CRISP provide summaries or abstracts.

Genet Med. 2002 Jan-Feb;4(1):20-6. PubMed citation • Ogino S, Wilson RB. Genetic testing and risk assessment for spinal muscular atrophy (SMA). Hum Genet. 2002 Dec;111(6):477-500. Epub 2002 Oct 03. Review. PubMed citation • Ogino S, Wilson RB. Spinal muscular atrophy: molecular genetics and diagnostics. Expert Rev Mol Diagn. 2004 Jan;4(1):15-29. PubMed citation • Prior TW, Swoboda KJ, Scott HD, Hejmanowski AQ. Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2.

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Amyotrophic Lateral Sclerosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker

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